Canonical Allele Identifier: PA916031564
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482661
ClinVar RCV Id: RCV000561901 RCV001238128 RCV002281114
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly330Ala
CA6264715
NM_001351834.2:c.989G>C