Allele Registry

Canonical Allele Identifier: PA2826634071

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000219938

RCV000459481

RCV001810439

RCV003316228

ClinVar Variation:

233214

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg1032Pro	CA10578173 NM_001281493.2:c.3095G>C