Canonical Allele Identifier: PA322656
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215329
ClinVar RCV Id: RCV000198166
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Gly120Ser
CA322653
NM_001257988.1:c.358G>A