Canonical Allele Identifier: PA2826450096
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2157816
ClinVar RCV Id: RCV003093382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Ala331Thr
CA325560833
NM_001257989.1:c.991G>A