Canonical Allele Identifier: PA916031986
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu651Pro
CA382536697
NM_001351834.2:c.1952T>C