Allele Registry

Canonical Allele Identifier: PA2573061711

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001757554

ClinVar Variation:

1316107

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu493Asp	CA346746022 NM_000179.3:c.1479G>C CA346746024 NM_000179.3:c.1479G>T