Canonical Allele Identifier: PA916031557
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453766
ClinVar RCV Id: RCV000528412 RCV000708662 RCV003470689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile326Val
CA382531103
NM_001351834.2:c.976A>G