Canonical Allele Identifier: PA2580252685
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2202100
ClinVar RCV Id: RCV002664001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Arg109Cys
CA325565295
NM_001953.5:c.325C>T