Allele Registry

Canonical Allele Identifier: PA1139674146

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001040752

RCV002409390

RCV003461455

ClinVar Variation:

839071

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu619Lys	CA346749766 NM_000179.3:c.1855G>A