ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA326693
Gene: CFTR
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000577469
RCV001001757
RCV001009543
RCV001284132
RCV003473468
ClinVar Variation:
53398
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000483.3:p.His609Arg
CA326692
NM_000492.4:c.1826A>G