Canonical Allele Identifier: PA645390601
Gene: CFAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 262555
ClinVar RCV Id: RCV000243043 RCV000650507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659457.2:p.Trp205Cys
CA8962350
NM_145020.5:c.615G>C
CA402441096
NM_145020.5:c.615G>T