Allele Registry

Canonical Allele Identifier: PA2825087899

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002003501

ClinVar Variation:

1486313

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu396Phe	CA346742399 NM_000179.3:c.1186C>T