Allele Registry

Canonical Allele Identifier: PA2826464069

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000487340

RCV001010926

RCV001030709

RCV001851231

RCV004003373

ClinVar Variation:

422351

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro373Ala	CA16617576 NM_001258281.1:c.1117C>G