Canonical Allele Identifier: PA210393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89506
ClinVar RCV Id: RCV000074974 RCV000160701 RCV000202090 RCV000491705 RCV000542786 RCV000576708 RCV001355904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1334Gln
CA015202
NM_000179.3:c.4001G>A