Allele Registry

Canonical Allele Identifier: PA915984141

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

133101

ClinVar RCV:

RCV000115528

RCV000195415

RCV000212583

RCV000524406

RCV000986649

RCV001353804

RCV001719858

RCV003492474

ClinVar Variation:

127644

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu62Val	CA021100 NM_001258281.1:c.184C>G