Allele Registry

Canonical Allele Identifier: PA167914

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131285

RCV000479474

RCV000548616

RCV002509239

RCV003998097

ClinVar Variation:

142264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser459Cys	CA008555 NM_000179.3:c.1376C>G