Canonical Allele Identifier: PA2829364522
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1451054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Val427Leu
CA325560322
NM_001953.5:c.1279G>C
CA412196735
NM_001953.5:c.1279G>T