Canonical Allele Identifier: PA1139676503
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 835227
ClinVar RCV Id: RCV001036059 RCV002400216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg55Pro
CA346728979
NM_000251.3:c.164G>C