Allele Registry

Canonical Allele Identifier: PA2825088583

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398931

ClinVar Variation:

1778592

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly571Ala	CA346748588 NM_000179.3:c.1712G>C