Allele Registry

Canonical Allele Identifier: PA2826464192

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000550095

RCV000575666

RCV001755785

RCV004003733

RCV004527635

ClinVar Variation:

455490

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu403Val	CA028542 NM_001258281.1:c.1207C>G