Canonical Allele Identifier: PA2573315036
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1347764
ClinVar RCV Id: RCV002050674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954986.2:p.Gln377His
CA5818409
NM_199292.3:c.1131G>C
CA379125941
NM_199292.3:c.1131G>T