Allele Registry

Canonical Allele Identifier: PA287340

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115437

RCV001071512

RCV001190341

RCV003467043

RCV003997254

ClinVar Variation:

127603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val215Gly	CA016108 NM_000179.3:c.644T>G