Canonical Allele Identifier: PA2825033951
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1449716
ClinVar RCV Id: RCV002004678
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1780Tyr
CA382543137
NM_000051.4:c.5339T>A