Allele Registry

Canonical Allele Identifier: PA2825091872

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001372799

ClinVar Variation:

1063009

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1196Lys	CA46717430 NM_000179.3:c.3586G>A