Canonical Allele Identifier: PA2828578819
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 376166
ClinVar RCV Id: RCV000430977 RCV000440400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362249.1:p.Tyr571Asp
CA16602623
NM_001375320.1:c.1711T>G