Canonical Allele Identifier: PA2826450159
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1433097
ClinVar RCV Id: RCV001944252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Asp386Tyr
CA10321474
NM_001257989.1:c.1156G>T