Canonical Allele Identifier: PA188561
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184308
ClinVar RCV Id: RCV000163537 RCV000484226 RCV000657098 RCV000794229 RCV003467279 RCV003995260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His610Tyr
CA019408
NM_000251.3:c.1828C>T