Canonical Allele Identifier: PA2499230082
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037505
ClinVar RCV Id: RCV001340669 RCV003469568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile666Val
CA346728936
NM_000251.3:c.1996A>G