Allele Registry

Canonical Allele Identifier: PA2826632771

Gene: MSH6 HGNC NCBI

ClinVar Allele:

1041568

ClinVar RCV:

RCV001362873

RCV003355435

RCV004005289

ClinVar Variation:

1054381

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg766Gly	CA46715775 NM_001281493.2:c.2296C>G