Allele Registry

Canonical Allele Identifier: PA330416

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074718

RCV001530136

RCV001854277

RCV003137606

RCV003584540

ClinVar Variation:

89254

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe706Ser	CA009702 NM_000179.3:c.2117T>C