Allele Registry

Canonical Allele Identifier: PA1139677130

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001207699

ClinVar Variation:

938476

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln183Glu	CA346730871 NM_000251.3:c.547C>G