Allele Registry

Canonical Allele Identifier: PA2580118498

Gene: CNTF HGNC NCBI

ClinVar Allele:

2264604

ClinVar RCV:

RCV004132615

ClinVar Variation:

2284727

HGVS (amino-acid)	Matching Registered Transcripts
NP_000605.1:p.Ile194Val	CA380754200 NM_000614.4:c.580A>G