Allele Registry

Canonical Allele Identifier: PA916011388

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

151013

ClinVar RCV:

RCV000129766

RCV000409325

RCV000464994

RCV000515187

RCV000586138

RCV001175358

RCV003153418

RCV003467119

RCV003997523

ClinVar Variation:

141299

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro952Ser	CA012124 NM_001281492.2:c.2854C>T