Canonical Allele Identifier: PA324947
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_001244918.1:p.Ala134Val
CA324943
NM_001257989.1:c.401C>T