Allele Registry

Canonical Allele Identifier: PA2826637691

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003461944

ClinVar Variation:

2676808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser893Gly	CA346760519 NM_001281494.2:c.2677A>G