Canonical Allele Identifier: PA2573068007
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1315419
ClinVar RCV Id: RCV001774669
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gln434Leu
CA325560311
NM_001257989.1:c.1301A>T