Allele Registry

Canonical Allele Identifier: PA2825088285

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003026792

ClinVar Variation:

2107070

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala494Gly	CA346746045 NM_000179.3:c.1481C>G