Allele Registry

Canonical Allele Identifier: PA196771

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000166804

RCV000701255

RCV003995533

ClinVar Variation:

187114

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro1110Ser	CA012609 NM_000179.3:c.3328C>T