Canonical Allele Identifier: PA2573203082
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1502681
ClinVar RCV Id: RCV002011051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr1844Ser
CA382545871
NM_001351834.2:c.5531A>C