Canonical Allele Identifier: PA2825035859
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2836901
ClinVar RCV Id: RCV003606550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2639Arg
CA6266212
NM_000051.4:c.7916A>G