ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825568538
Gene: TYMP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2138462
ClinVar RCV Id:
RCV003050585
RCV003147815
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107228.1:p.Leu347Pro
CA412197822
NM_001113756.3:c.1040T>C