Canonical Allele Identifier: PA2826217591
Gene: CFAP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 31150
ClinVar RCV Id: RCV000024146
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182760.2:p.Asp523Tyr
CA129719
NM_001195831.3:c.1567G>T