Allele Registry

Canonical Allele Identifier: PA2826625954

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003026792

ClinVar Variation:

2107070

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ala364Gly	CA346746045 NM_001281492.2:c.1091C>G