Allele Registry

Canonical Allele Identifier: PA2825092111

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001178948

RCV001361175

ClinVar Variation:

920280

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1235Phe	CA346760985 NM_000179.3:c.3703C>T