Canonical Allele Identifier: PA2573164935
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427368
ClinVar RCV Id: RCV001933671
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala306Ile
CA2573134973
NM_000251.3:c.916_917delinsAT