Allele Registry

Canonical Allele Identifier: PA331213

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076008

RCV000490568

RCV000680197

RCV002399451

ClinVar Variation:

90513

561171

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Pro349Arg	CA016981 NM_000251.3:c.1046C>G CA658822113 NM_000251.3:c.1046_1047delinsGC