Canonical Allele Identifier: PA2825033002
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1438048
ClinVar RCV Id: RCV001948881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu1353Lys
CA382528009
NM_000051.4:c.4057G>A