Canonical Allele Identifier: PA2828579135
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2111958
ClinVar RCV Id: RCV003024094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Asn172Asp
CA361724882
NM_001375321.1:c.514A>G