Canonical Allele Identifier: PA165919
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89270
ClinVar RCV Id: RCV000130193 RCV003997074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Trp777Arg
CA010044
NM_000179.3:c.2329T>A
CA346753332
NM_000179.3:c.2329T>C