Allele Registry

Canonical Allele Identifier: PA2826635008

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491862

RCV000822280

RCV003464048

RCV004003456

ClinVar Variation:

428340

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser234Thr	CA346746995 NM_001281494.2:c.701G>C