Canonical Allele Identifier: PA2580253011
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_001944.1:p.Ala333Val
CA412198041
NM_001953.5:c.998C>T