Canonical Allele Identifier: PA2825568331
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 16660
ClinVar RCV Id: RCV000018140 RCV001052862 RCV001826476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly153Ser
CA126774
NM_001113756.3:c.457G>A