Canonical Allele Identifier: PA2828579152
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1360911
ClinVar RCV Id: RCV001865065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.His214Cys
CA2573139287
NM_001375321.1:c.640_641delinsTG