Allele Registry

Canonical Allele Identifier: PA196972

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000166896

RCV000472836

RCV000590192

RCV000662856

RCV003995543

RCV004535130

ClinVar Variation:

187194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser323Phe	CA022667 NM_000251.3:c.968C>T