Canonical Allele Identifier: PA2741867656
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2836901
ClinVar RCV Id: RCV003606550
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2639Arg
CA6266212
NM_001351834.2:c.7916A>G