Canonical Allele Identifier: PA2826712677
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2795626
ClinVar RCV Id: RCV003675546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275634.1:p.Pro347Leu
CA361724501
NM_001288705.3:c.1040C>T