Canonical Allele Identifier: PA2741814997
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2506208
ClinVar RCV Id: RCV003236439
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val1153Leu
CA368993709
NM_000492.4:c.3457G>T
CA368993711
NM_000492.4:c.3457G>C