Canonical Allele Identifier: PA916031649
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys387Arg
CA10578996
NM_001351834.2:c.1160A>G