Canonical Allele Identifier: PA2825035977
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1041810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2694Ala
CA382562030
NM_000051.4:c.8081G>C