Allele Registry

Canonical Allele Identifier: PA658680144

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000571824

RCV001858112

ClinVar Variation:

479956

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr118Lys	CA071156 NM_000179.3:c.353C>A