Canonical Allele Identifier: PA645391688
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235131
ClinVar RCV Id: RCV000223936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653197.2:p.Gln449His
CA10581229
NM_144596.4:c.1347G>C
CA390553557
NM_144596.4:c.1347G>T