Canonical Allele Identifier: PA332427
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135856
ClinVar Variation Id: 1213458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln662His
CA019664
NM_000251.3:c.1986G>C
CA346728893
NM_000251.3:c.1986G>T