Canonical Allele Identifier: PA1139727732
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 958260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2307Val
CA382557078
NM_001351834.2:c.6919C>G