Allele Registry

Canonical Allele Identifier: PA337554

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

212214

221251

ClinVar RCV:

RCV000197947

RCV000204112

RCV000484712

RCV000561391

RCV000575386

RCV000663157

RCV000765676

RCV000765677

RCV003996993

RCV003997571

ClinVar Variation:

216296

219577

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly46Arg	CA337552 NM_000179.3:c.136G>C CA348361 NM_000179.3:c.136G>A