Allele Registry

Canonical Allele Identifier: PA916011380

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000074823

RCV000162445

RCV000254700

RCV000524159

RCV000709742

RCV000780464

RCV001356266

RCV001564011

RCV003162475

RCV003466947

RCV003492400

RCV003997086

ClinVar Variation:

89357

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg946Cys	CA012063 NM_001281492.2:c.2836C>T