Canonical Allele Identifier: PA2573202167
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1438048
ClinVar RCV Id: RCV001948881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu1353Lys
CA382528009
NM_001351834.2:c.4057G>A