Canonical Allele Identifier: PA2825195467
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231912
ClinVar RCV Id: RCV004518627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn1419Lys
CA368984423
NM_000492.4:c.4257C>A
CA368984426
NM_000492.4:c.4257C>G