Canonical Allele Identifier: PA2825568654
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1315419
ClinVar RCV Id: RCV001774669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gln429Leu
CA325560311
NM_001113756.3:c.1286A>T