Canonical Allele Identifier: PA658736774
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491837
ClinVar RCV Id: RCV000583255 RCV000691466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr238Cys
CA346732073
NM_000251.3:c.713A>G