Allele Registry

Canonical Allele Identifier: PA299519

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000205769

RCV000491170

RCV000587383

RCV000663327

ClinVar Variation:

182660

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr750Lys	CA009894 NM_000179.3:c.2249C>A