Allele Registry

Canonical Allele Identifier: PA354454

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000201977

RCV000205853

RCV000491320

RCV000656880

RCV003226247

RCV003462356

ClinVar Variation:

218040

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg621Leu	CA210371 NM_000251.3:c.1862G>T