Canonical Allele Identifier: PA645407137
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223020
ClinVar RCV Id: RCV000208698
ClinVar Variation Id: 223021
ClinVar RCV Id: RCV000208640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Glu87Asp
CA10321803
NM_001953.5:c.261G>C
CA16616773
NM_001953.5:c.261G>T