Allele Registry

Canonical Allele Identifier: PA330559

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216969

RCV000684809

RCV000767045

RCV003460689

RCV004017385

ClinVar Variation:

89449

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1242Ser	CA014030 NM_000179.3:c.3724C>A