Canonical Allele Identifier: PA2826746888
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275880.1:p.Lys606Arg
CA060659
NM_001288951.2:c.1817A>G