Allele Registry

Canonical Allele Identifier: PA2826625817

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003364334

ClinVar Variation:

2609841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly330Cys	CA346744970 NM_001281492.2:c.988G>T