Canonical Allele Identifier: PA2741865694
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2577565
ClinVar RCV Id: RCV003324902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu233Val
CA382529104
NM_001351834.2:c.697T>G