Canonical Allele Identifier: PA2826449296
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163693
ClinVar RCV Id: RCV001508953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Ser30Leu
CA10321883
NM_001257988.1:c.89C>T