Canonical Allele Identifier: PA916033598
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524316
ClinVar RCV Id: RCV000628014 RCV000777922
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys1899Arg
CA6265758
NM_001351834.2:c.5695T>C