Canonical Allele Identifier: PA2573187641
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1611579
ClinVar RCV Id: RCV002148128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Pro388Ser
CA412197190
NM_001257989.1:c.1162C>T