Canonical Allele Identifier: PA2573187664
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1451054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Val432Leu
CA325560322
NM_001257989.1:c.1294G>C
CA412196735
NM_001257989.1:c.1294G>T