Canonical Allele Identifier: PA325690
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35821
ClinVar RCV Id: RCV000029474 RCV000731635 RCV001001125 RCV001009542 RCV001331274 RCV000763570 RCV001004447 RCV003473123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val456Ala
CA325689
NM_000492.4:c.1367T>C