Canonical Allele Identifier: PA168426
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142464
ClinVar RCV Id: RCV000131596 RCV000805430 RCV002466443 RCV002466444
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala70Val
CA020016
NM_000251.3:c.209C>T