Canonical Allele Identifier: PA2573165050
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692297
ClinVar RCV Id: RCV002259214 RCV003315452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys235Thr
CA346732011
NM_000251.3:c.704A>C