Canonical Allele Identifier: PA2828212632
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 531831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353464.1:p.Arg433Trp
CA7302713
NM_001366535.2:c.1297C>T