Canonical Allele Identifier: PA658671857
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455611
ClinVar RCV Id: RCV000536657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu241Val
CA346732141
NM_000251.3:c.721C>G