Canonical Allele Identifier: PA2825883819
Gene: CFP HGNC NCBI

Linked Data

ClinVar Variation Id: 1991793
ClinVar RCV Id: RCV002776407
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138724.1:p.Gly138Ser
CA10398959
NM_001145252.3:c.412G>A