Canonical Allele Identifier: PA327501
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53955
ClinVar RCV Id: RCV000577102
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met152Val
CA327500
NM_000492.4:c.454A>G