Canonical Allele Identifier: PA658670559
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453707
ClinVar RCV Id: RCV000559858 RCV002413420
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2618Gly
CA382561371
NM_000051.4:c.7852A>G