Canonical Allele Identifier: PA167887
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135865
ClinVar RCV Id: RCV000122993 RCV000131260 RCV000237042 RCV000409770 RCV000656875 RCV003997410
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu279Val
CA022395
NM_000251.3:c.835C>G