Canonical Allele Identifier: PA321069
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215328
ClinVar RCV Id: RCV000196647 RCV001273320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Ala94Val
CA321064
NM_001953.5:c.281C>T