Canonical Allele Identifier: PA2825568645
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2109216
ClinVar RCV Id: RCV003038246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Leu424Val
CA412196788
NM_001113756.3:c.1270C>G