Canonical Allele Identifier: PA916034470
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2580Lys
CA6266172
NM_001351834.2:c.7739G>A