Canonical Allele Identifier: PA2825568317
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215330
ClinVar RCV Id: RCV000676464 RCV001145863 RCV001273319
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Ala134Val
CA324943
NM_001113756.3:c.401C>T