Canonical Allele Identifier: PA2826449589
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2023066
ClinVar RCV Id: RCV002852960
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Ala333Val
CA412198041
NM_001257988.1:c.998C>T