Allele Registry

Canonical Allele Identifier: PA192035

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164895

RCV000663227

RCV001037948

RCV002255308

RCV002281982

RCV003995375

ClinVar Variation:

185467

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.His578Tyr	CA009101 NM_000179.3:c.1732C>T