Allele Registry

Canonical Allele Identifier: PA916011063

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074698

RCV000160709

RCV000524128

RCV000568962

ClinVar Variation:

89234

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser65Leu	CA009482 NM_001281492.2:c.194C>T