Canonical Allele Identifier: PA916032162
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 821191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn796Ser
CA382541056
NM_001351834.2:c.2387A>G