Allele Registry

Canonical Allele Identifier: PA2825088844

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002413091

ClinVar Variation:

1781404

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu619Gly	CA346749772 NM_000179.3:c.1856A>G