Canonical Allele Identifier: PA2741814736
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2587599
ClinVar RCV Id: RCV003350763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala763Ser
CA368980855
NM_000492.4:c.2287G>T