Canonical Allele Identifier: PA2825031789
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1791707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala823Pro
CA382543087
NM_000051.4:c.2467G>C