Canonical Allele Identifier: PA916034122
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482702
ClinVar RCV Id: RCV000573901 RCV002530300
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2302Arg
CA382556982
NM_001351834.2:c.6905A>G