Allele Registry

Canonical Allele Identifier: PA334058

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000167959

RCV000409734

RCV000491880

RCV000759851

RCV003468820

RCV003995600

ClinVar Variation:

188107

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu735Ile	CA009870 NM_000179.3:c.2203C>A