Canonical Allele Identifier: PA2825883826
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 1505433
ClinVar RCV Id: RCV002035749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138724.1:p.Arg157Trp
CA10398954
NM_001145252.3:c.469C>T