Canonical Allele Identifier: PA916034760
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 661938
ClinVar RCV Id: RCV001017656 RCV000819464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe2796Leu
CA382516578
NM_001351834.2:c.8386T>C
CA382516596
NM_001351834.2:c.8388C>A
CA382516601
NM_001351834.2:c.8388C>G