Canonical Allele Identifier: PA916032388
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser934Arg
CA10579070
NM_001351834.2:c.2802C>G
CA382545660
NM_001351834.2:c.2800A>C
CA382545671
NM_001351834.2:c.2802C>A