Allele Registry

Canonical Allele Identifier: PA2826628443

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000217088

RCV000475398

RCV000482975

RCV000662884

RCV003997945

ClinVar Variation:

232091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Met1026Thr	CA10578145 NM_001281492.2:c.3077T>C