Canonical Allele Identifier: PA2580181610
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2109216
ClinVar RCV Id: RCV003038246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Leu429Val
CA412196788
NM_001257989.1:c.1285C>G