Canonical Allele Identifier: PA915956627
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 638165
ClinVar RCV Id: RCV000790623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln372His
CA368979126
NM_000492.4:c.1116G>C
CA368979127
NM_000492.4:c.1116G>T