Canonical Allele Identifier: PA2825151534
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2679202
ClinVar RCV Id: RCV003474117
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000351.2:p.Arg214Met
CA216286476
NM_000360.3:c.641G>T