Canonical Allele Identifier: PA2573315075
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1384057
ClinVar RCV Id: RCV001895709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Met30Ile
CA5818867
NM_199293.3:c.90G>A
CA379112754
NM_199293.3:c.90G>T
CA379112755
NM_199293.3:c.90G>C