Canonical Allele Identifier: PA916032042
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg692His
CA6264924
NM_001351834.2:c.2075G>A