Canonical Allele Identifier: PA121400
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 11183
ClinVar RCV Id: RCV000011933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002612.1:p.Gly298Val
CA121398
NM_002621.2:c.893G>T