Allele Registry

Canonical Allele Identifier: PA915984348

Gene: MSH2 HGNC NCBI

ClinVar Allele:

185977

ClinVar RCV:

RCV000167977

RCV000223301

RCV000240465

RCV003454423

ClinVar Variation:

188119

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly98Glu	CA021218 NM_001258281.1:c.293G>A