Allele Registry

Canonical Allele Identifier: PA2826632715

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

94816

ClinVar RCV:

RCV000218375

RCV000409200

RCV000565213

RCV000627700

RCV000764427

RCV003460677

RCV003493433

ClinVar Variation:

89342

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ala753Thr	CA011694 NM_001281493.2:c.2257G>A