ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2825568304
Gene: TYMP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
215329
ClinVar RCV Id:
RCV000198166
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107228.1:p.Gly120Ser
CA322653
NM_001113756.3:c.358G>A