Canonical Allele Identifier: PA2826449398
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2150999
ClinVar RCV Id: RCV003072020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Ala130Val
CA412201953
NM_001257988.1:c.389C>T