Canonical Allele Identifier: PA190121
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184810
ClinVar RCV Id: RCV000164134 RCV000525136 RCV001193893 RCV001762365 RCV003462126 RCV003995317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly25Asp
CA022180
NM_000251.3:c.74G>A