Canonical Allele Identifier: PA2825567973
Gene: TYMP HGNC NCBI
ClinVar Allele:
224798
ClinVar RCV:
RCV000208647
ClinVar Variation:
223073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.Ala332_Gly337dup