Allele Registry

Canonical Allele Identifier: PA658672513

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.4063973032

ClinVar RCV:

RCV000572647

RCV000686725

ClinVar Variation:

483701

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp506Glu	CA346727718 NM_000251.3:c.1518C>G CA346727719 NM_000251.3:c.1518C>A