Allele Registry

Canonical Allele Identifier: PA2826635370

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001040752

RCV002409390

RCV003461455

ClinVar Variation:

839071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu317Lys	CA346749766 NM_001281494.2:c.949G>A