Canonical Allele Identifier: PA193090
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185830
ClinVar RCV Id: RCV000165325 RCV000537745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg791Cys
CA010130
NM_000179.3:c.2371C>T