Canonical Allele Identifier: PA916033901
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407649
ClinVar RCV Id: RCV000463293 RCV000478293 RCV000562429 RCV003470432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Trp2109Gly
CA16613408
NM_001351834.2:c.6325T>G