Canonical Allele Identifier: PA2573204582
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1382708
ClinVar RCV Id: RCV001890490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2896Arg
CA382523600
NM_001351834.2:c.8687A>G