Allele Registry

Canonical Allele Identifier: PA299300

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.348590375

ClinVar RCV:

RCV000160578

RCV000203837

RCV002444666

RCV003467247

ClinVar Variation:

182555

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met300Val	CA022496 NM_000251.3:c.898A>G