ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825568121
Gene: TYMP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2418087
ClinVar RCV Id:
RCV003118196
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107227.1:p.Arg442Trp
CA412196452
NM_001113755.3:c.1324C>T