Allele Registry

Canonical Allele Identifier: PA194762

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000166008

RCV000679237

RCV001085290

RCV001264551

RCV003995471

ClinVar Variation:

186416

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe11Leu	CA012766 NM_000179.3:c.33C>G CA346734518 NM_000179.3:c.31T>C CA346734523 NM_000179.3:c.33C>A