Allele Registry

Canonical Allele Identifier: PA2826630662

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164895

RCV000663227

RCV001037948

RCV002255308

RCV002281982

RCV003995375

ClinVar Variation:

185467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.His276Tyr	CA009101 NM_001281493.2:c.826C>T