Canonical Allele Identifier: PA2579922086
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790465
ClinVar RCV Id: RCV002457918
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro795Ser
CA346730119
NM_000251.3:c.2383C>T