Allele Registry

Canonical Allele Identifier: PA1139672163

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001239065

RCV004034595

ClinVar Variation:

964772

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln236Glu	CA346739981 NM_000179.3:c.706C>G