Canonical Allele Identifier: PA2826449377
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2202100
ClinVar RCV Id: RCV002664001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Arg109Cys
CA325565295
NM_001257988.1:c.325C>T