Allele Registry

Canonical Allele Identifier: PA2826465140

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000167253

RCV000490613

RCV000817438

RCV001270946

ClinVar Variation:

187518

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Cys631Tyr	CA019995 NM_001258281.1:c.1892G>A