Canonical Allele Identifier: PA095114
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91267
ClinVar RCV Id: RCV000129083 RCV000236043 RCV000656871 RCV000662483 RCV000627734 RCV001354855 RCV002483125 RCV003997185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr33Pro
CA022692
NM_000251.3:c.97A>C