Canonical Allele Identifier: PA916031848
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 570803
ClinVar RCV Id: RCV000691757
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala545Thr
CA382534518
NM_001351834.2:c.1633G>A