Canonical Allele Identifier: PA916033046
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 641120
ClinVar RCV Id: RCV000794287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1446Asp
CA382531940
NM_001351834.2:c.4337T>A