Allele Registry

Canonical Allele Identifier: PA194896

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000166062

RCV000228645

RCV000589227

RCV000662660

RCV001357474

RCV003995476

ClinVar Variation:

186463

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp41Glu	CA017623 NM_000251.3:c.123C>G CA346728848 NM_000251.3:c.123C>A