Canonical Allele Identifier: PA2826520267
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 2004927
ClinVar RCV Id: RCV002820648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258369.1:p.Trp93Cys
CA410456739
NM_001271440.2:c.279G>T
CA410456744
NM_001271440.2:c.279G>C