Allele Registry

Canonical Allele Identifier: PA2826633348

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003461944

ClinVar Variation:

2676808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser893Gly	CA346760519 NM_001281493.2:c.2677A>G