Canonical Allele Identifier: PA2826745014
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 314797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275710.1:p.Ser2Asn
CA7302304
NM_001288781.1:c.5G>A