Canonical Allele Identifier: PA2825883830
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 1475060
ClinVar RCV Id: RCV001973840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138724.1:p.Arg159Cys
CA412838718
NM_001145252.3:c.475C>T