Allele Registry

Canonical Allele Identifier: PA2825090835

Gene: MSH6 HGNC NCBI

ClinVar Allele:

1041568

ClinVar RCV:

RCV001362873

RCV003355435

RCV004005289

ClinVar Variation:

1054381

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1068Gly	CA46715775 NM_000179.3:c.3202C>G