Canonical Allele Identifier: PA2741814603
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2562516
ClinVar RCV Id: RCV003296509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn538His
CA368975941
NM_000492.4:c.1612A>C