Allele Registry

Canonical Allele Identifier: PA287346

Gene: MSH6 HGNC NCBI

ClinVar Allele:

133062

ClinVar RCV:

RCV000115443

RCV000212634

RCV000685169

RCV003997256

ClinVar Variation:

127605

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly273Arg	CA016493 NM_000179.3:c.817G>A CA346740406 NM_000179.3:c.817G>C