Allele Registry

Canonical Allele Identifier: PA2826463039

Gene: MSH2 HGNC NCBI

ClinVar Allele:

152609

ClinVar RCV:

RCV000132363

RCV000629706

RCV003998144

ClinVar Variation:

142895

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro130Ser	CA021484 NM_001258281.1:c.388C>T