Canonical Allele Identifier: PA2826465383
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229891
ClinVar RCV Id: RCV000215978 RCV001222233 RCV003454615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp692Tyr
CA10578001
NM_001258281.1:c.2074G>T