Canonical Allele Identifier: PA916031558
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 644776
ClinVar RCV Id: RCV000798766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly327Glu
CA382531144
NM_001351834.2:c.980G>A