Canonical Allele Identifier: PA2826449712
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1451054
ClinVar RCV Id: RCV002007113 RCV003170161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Val427Leu
CA325560322
NM_001257988.1:c.1279G>C
CA412196735
NM_001257988.1:c.1279G>T