Canonical Allele Identifier: PA2499230045
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002257
ClinVar RCV Id: RCV001298657
ClinVar Variation Id: 1055457
ClinVar RCV Id: RCV002420799 RCV001364129
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln690His
CA346729181
NM_000251.3:c.2070A>C
CA346729182
NM_000251.3:c.2070A>T