Allele Registry

Canonical Allele Identifier: PA2826465409

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000491833

RCV000684788

ClinVar Variation:

90950

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Trp698Cys	CA020440 NM_001258281.1:c.2094G>C CA346729840 NM_001258281.1:c.2094G>T