Canonical Allele Identifier: PA327567
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 558712
ClinVar RCV Id: RCV000675021 RCV001193645 RCV003472180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn186Lys
CA327566
NM_000492.4:c.558C>A
CA368976532
NM_000492.4:c.558C>G