Canonical Allele Identifier: PA2828212700
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 262515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353465.1:p.Asp55Gly
CA7302389
NM_001366536.2:c.164A>G