Canonical Allele Identifier: PA2579918796
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780213
ClinVar RCV Id: RCV002404225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val598Leu
CA346728310
NM_000251.3:c.1792G>T
CA346728311
NM_000251.3:c.1792G>C