Allele Registry

Canonical Allele Identifier: PA287342

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115441

RCV000410116

RCV000466432

RCV000566072

RCV003467044

RCV003997255

ClinVar Variation:

127604

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu228Lys	CA016246 NM_000179.3:c.682G>A