Canonical Allele Identifier: PA2825192599
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231927
ClinVar RCV Id: RCV004518642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn187His
CA368976534
NM_000492.4:c.559A>C