Canonical Allele Identifier: PA2573170571
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1470640
ClinVar RCV Id: RCV001995271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val397Leu
CA368980198
NM_000492.4:c.1189G>C
CA368980201
NM_000492.4:c.1189G>T