Canonical Allele Identifier: PA2829663397
Gene: IFT27 HGNC NCBI
ClinVar RCV:
RCV001063722
ClinVar Variation:
857948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006851.1:p.Val153Met
CA10212339
NM_006860.5:c.457G>A