Canonical Allele Identifier: PA645501566
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407624
ClinVar Variation Id: 1727708
ClinVar RCV Id: RCV002326048
ClinVar Variation Id: 1983990
ClinVar RCV Id: RCV002770569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1036Leu
CA6265196
NM_000051.4:c.3106T>C
CA382515149
NM_000051.4:c.3108C>G
CA382515152
NM_000051.4:c.3108C>A