Allele Registry

Canonical Allele Identifier: PA2826632923

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129716

RCV000222346

RCV001089139

RCV003997519

ClinVar Variation:

141274

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr798Arg	CA012463 NM_001281493.2:c.2393C>G