Canonical Allele Identifier: PA2579910395
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 822657
ClinVar RCV Id: RCV001018181 RCV001860896
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu101Gly
CA346729631
NM_000251.3:c.302A>G