Canonical Allele Identifier: PA916032537
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407624
ClinVar RCV Id: RCV000459438 RCV000566084 RCV001358008 RCV002481423 RCV003470427 RCV003477949 RCV003993968
ClinVar Variation Id: 1727708
ClinVar RCV Id: RCV002326048
ClinVar Variation Id: 1983990
ClinVar RCV Id: RCV002770569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1036Leu
CA6265196
NM_001351834.2:c.3106T>C
CA382515149
NM_001351834.2:c.3108C>G
CA382515152
NM_001351834.2:c.3108C>A