Canonical Allele Identifier: PA2826449361
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223020
ClinVar RCV Id: RCV000208698
ClinVar Variation Id: 223021
ClinVar RCV Id: RCV000208640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Glu87Asp
CA10321803
NM_001257988.1:c.261G>C
CA16616773
NM_001257988.1:c.261G>T