Canonical Allele Identifier: PA126778
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 16660
ClinVar RCV Id: RCV000018140 RCV001052862 RCV001826476
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gly153Ser
CA126774
NM_001257989.1:c.457G>A