Allele Registry

Canonical Allele Identifier: PA2826628539

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000469909

RCV000521217

RCV000568727

RCV000663017

RCV003463928

RCV004001826

ClinVar Variation:

410425

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu1047Val	CA071122 NM_001281492.2:c.3139C>G