Allele Registry

Canonical Allele Identifier: PA915963939

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001011252

RCV004004498

ClinVar Variation:

819040

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly460Ser	CA346744965 NM_000179.3:c.1378G>A