Canonical Allele Identifier: PA1139732335
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 920370
ClinVar RCV Id: RCV001179051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala216Pro
CA6264638
NM_001351834.2:c.646G>C