Canonical Allele Identifier: PA104949
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 11185
ClinVar RCV Id: RCV000011935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138724.1:p.Tyr414Asp
CA121405
NM_001145252.3:c.1240T>G