Allele Registry

Canonical Allele Identifier: PA658680279

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000535308

RCV000571023

RCV004003702

ClinVar Variation:

455342

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile245Val	CA346740050 NM_000179.3:c.733A>G