Allele Registry

Canonical Allele Identifier: PA1139690417

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001229724

ClinVar Variation:

956843

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu35Gln	CA346729628 NM_001258281.1:c.103G>C