Canonical Allele Identifier: PA916062556
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 526214
ClinVar RCV Id: RCV001273893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Asp5Asn
CA5818893
NM_199293.3:c.13G>A