Allele Registry

Canonical Allele Identifier: PA658803884

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000630037

RCV001026328

ClinVar Variation:

525763

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys246Glu	CA346732225 NM_000251.3:c.736A>G