Canonical Allele Identifier: PA916032040
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 657570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp691His
CA6264923
NM_001351834.2:c.2071G>C