Allele Registry

Canonical Allele Identifier: PA287270

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

94692

ClinVar RCV:

RCV000115381

RCV000409690

RCV000491847

RCV000524118

RCV003235029

RCV003466935

RCV003993789

RCV003997068

ClinVar Variation:

89218

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg577Cys	CA009088 NM_000179.3:c.1729C>T