Canonical Allele Identifier: PA2580146059
Gene: CFAP96 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233014
ClinVar RCV Id: RCV004550538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107829.1:p.Asp171Glu
CA112036129
NM_001114357.3:c.513T>G
CA358904261
NM_001114357.3:c.513T>A