Canonical Allele Identifier: PA2573071127
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1331909
ClinVar RCV Id: RCV001804425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys177Arg
CA382527582
NM_001351834.2:c.530A>G