Allele Registry

Canonical Allele Identifier: PA163539

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

150493

ClinVar RCV:

RCV000128922

RCV000220784

RCV000226897

RCV000412094

RCV000780475

RCV001356921

RCV003149883

RCV003153411

RCV003323293

RCV004532539

ClinVar Variation:

140779

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala36Val	CA007963 NM_000179.3:c.107C>T