Allele Registry

Canonical Allele Identifier: PA2826625848

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000074653

RCV000166488

RCV000222213

RCV000524109

RCV000587141

RCV001535649

RCV003450925

RCV004528269

ClinVar Variation:

89191

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg338Cys	CA008576 NM_001281492.2:c.1012C>T