Allele Registry

Canonical Allele Identifier: PA645510798

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164110

RCV000466573

RCV000506000

RCV000589252

RCV000663282

ClinVar Variation:

184794

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Val858Phe	CA013053 NM_001281493.2:c.2572G>T