Canonical Allele Identifier: PA2579921973
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790186
ClinVar RCV Id: RCV002457714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr788Ser
CA346730014
NM_000251.3:c.2362A>T
CA346730020
NM_000251.3:c.2363C>G