Allele Registry

Canonical Allele Identifier: PA1139673282

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001200626

ClinVar Variation:

932698

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu493Lys	CA346745983 NM_000179.3:c.1477G>A