Canonical Allele Identifier: PA2828212926
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 314804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353465.1:p.Ala420Val
CA7302781
NM_001366536.2:c.1259C>T