Canonical Allele Identifier: PA2829384166
Gene: MSH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 417969
ClinVar RCV Id: RCV000477966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002432.1:p.Asp487Tyr
CA16616947
NM_002441.5:c.1459G>T