Canonical Allele Identifier: PA2741866493
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2576398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp851His
CA382543720
NM_001351834.2:c.2551G>C