Allele Registry

Canonical Allele Identifier: PA2826465184

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

180023

ClinVar RCV:

RCV000160602

RCV000410402

RCV000491763

RCV000761096

RCV001085231

RCV001193853

RCV001354130

ClinVar Variation:

182571

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Cys641Tyr	CA020070 NM_001258281.1:c.1922G>A