Canonical Allele Identifier: PA916034732
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420015
ClinVar RCV Id: RCV000486226 RCV000670258 RCV000565973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2772Arg
CA16619256
NM_001351834.2:c.8314G>A
CA382516367
NM_001351834.2:c.8314G>C