Allele Registry

Canonical Allele Identifier: PA2826626473

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000165560

RCV000168072

RCV000479956

RCV002469035

RCV003462180

RCV003995427

ClinVar Variation:

186038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Cys485Phe	CA009321 NM_001281492.2:c.1454G>T