Canonical Allele Identifier: PA645498533
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230853
ClinVar RCV Id: RCV000217038 RCV000235397 RCV001069719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly197Arg
CA6264633
NM_000051.4:c.589G>A
CA382528000
NM_000051.4:c.589G>C