Canonical Allele Identifier: PA2580203940
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1737799
ClinVar RCV Id: RCV002323289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1367Tyr
CA382528592
NM_001351834.2:c.4099G>T