Allele Registry

Canonical Allele Identifier: PA658804082

Gene: MSH2 HGNC NCBI

MaveDb:

Score 0.4909098393

ClinVar Allele:

518447

ClinVar RCV:

RCV000629968

RCV000777516

ClinVar Variation:

525729

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg711Leu	CA346729289 NM_000251.3:c.2132G>T