Canonical Allele Identifier: PA915962683
Gene: CNTF HGNC NCBI

Linked Data

ClinVar Variation Id: 768450
ClinVar RCV Id: RCV000947349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000605.1:p.Asn49Ser
CA6014993
NM_000614.4:c.146A>G