Allele Registry

Canonical Allele Identifier: PA916011930

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000217088

RCV000475398

RCV000482975

RCV000662884

RCV003997945

ClinVar Variation:

232091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Met854Thr	CA10578145 NM_001281494.2:c.2561T>C