Allele Registry

Canonical Allele Identifier: PA645382902

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000231932

RCV000571874

RCV000581651

RCV001589169

RCV003463639

RCV003998722

RCV004529388

ClinVar Variation:

237168

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile944Val	CA10582071 NM_000179.3:c.2830A>G