Allele Registry

Canonical Allele Identifier: PA2826464330

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000572647

RCV000686725

ClinVar Variation:

483701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp440Glu	CA346727718 NM_001258281.1:c.1320C>G CA346727719 NM_001258281.1:c.1320C>A