Canonical Allele Identifier: PA916034038
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 627887
ClinVar RCV Id: RCV000771924 RCV001766600 RCV001856005
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2235Val
CA6265997
NM_001351834.2:c.6703A>G