Canonical Allele Identifier: PA1139753842
Gene: CSF3R HGNC NCBI

Linked Data

ClinVar Variation Id: 842556
ClinVar RCV Id: RCV001044992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_724781.1:p.Thr773Ile
CA339413538
NM_156039.3:c.2318C>T