Allele Registry

Canonical Allele Identifier: PA2826463358

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000236426

RCV000458697

RCV000564711

RCV001356679

RCV003998919

ClinVar Variation:

246308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val207Ile	CA040766 NM_001258281.1:c.619G>A