Canonical Allele Identifier: PA2825883822
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 2812320
ClinVar RCV Id: RCV003685352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138724.1:p.Lys154Arg
CA412838745
NM_001145252.3:c.461A>G