Canonical Allele Identifier: PA196010
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89191
ClinVar RCV Id: RCV000074653 RCV000166488 RCV000222213 RCV000524109 RCV000587141 RCV001535649 RCV003450925 RCV004528269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg468Cys
CA008576
NM_000179.3:c.1402C>T