Canonical Allele Identifier: PA658673571
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478985
ClinVar RCV Id: RCV000573160 RCV002527968
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp317Tyr
CA382530854
NM_000051.4:c.949G>T