Allele Registry

Canonical Allele Identifier: PA2826633541

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001178948

RCV001361175

ClinVar Variation:

920280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu933Phe	CA346760985 NM_001281493.2:c.2797C>T