Canonical Allele Identifier: PA645376271
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 321942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Arg52Gln
CA10649540
NM_017775.4:c.155G>A