Canonical Allele Identifier: PA1139734374
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 965804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe652Ser
CA6264912
NM_001351834.2:c.1955T>C