Canonical Allele Identifier: PA345395
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90714
ClinVar RCV Id: RCV000490983 RCV000479671 RCV000524350 RCV003317077 RCV003466965 RCV003997151
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly548Cys
CA018790
NM_000251.3:c.1642G>T