Canonical Allele Identifier: PA2828579263
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 376166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Tyr423Asp
CA16602623
NM_001375321.1:c.1267T>G