Canonical Allele Identifier: PA916032013
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly670Asp
CA228393595
NM_001351834.2:c.2009G>A