Canonical Allele Identifier: PA915984214
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231613
ClinVar RCV Id: RCV000221599 RCV000465648 RCV000483760 RCV000662917 RCV000780457 RCV003997912
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile79Val
CA10577937
NM_001258281.1:c.235A>G