Allele Registry

Canonical Allele Identifier: PA2826465073

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

96343

2840871

ClinVar RCV:

RCV000076370

RCV000132039

RCV000202225

RCV000524373

RCV001264415

RCV001588897

RCV003452883

RCV003455975

ClinVar Variation:

90868

2673350

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly617Arg	CA019900 NM_001258281.1:c.1849G>A CA346729142 NM_001258281.1:c.1849G>C