Allele Registry

Canonical Allele Identifier: PA287350

Gene: MSH6 HGNC NCBI

ClinVar Allele:

95047

ClinVar RCV:

RCV000075042

RCV000115445

RCV000212636

RCV000410872

RCV000512927

RCV000524217

ClinVar Variation:

89573

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys295Arg	CA016588 NM_000179.3:c.884A>G