Canonical Allele Identifier: PA916032035
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu686Ile
CA382537468
NM_001351834.2:c.2056C>A