Allele Registry

Canonical Allele Identifier: PA2826635187

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115381

RCV000409690

RCV000491847

RCV000524118

RCV003235029

RCV003466935

RCV003993789

RCV003997068

ClinVar Variation:

89218

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg275Cys	CA009088 NM_001281494.2:c.823C>T