Canonical Allele Identifier: PA1139732787
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 937558
ClinVar RCV Id: RCV001206595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr306Lys
CA382530546
NM_001351834.2:c.917C>A