Canonical Allele Identifier: PA2579922172
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790666
ClinVar RCV Id: RCV002450225 RCV003101788 RCV003455467 RCV004007426
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu800Pro
CA346730184
NM_000251.3:c.2399T>C