Canonical Allele Identifier: PA658816848
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 516796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Gln41Arg
CA398382480
NM_017775.4:c.122A>G