Canonical Allele Identifier: PA2828579145
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_001362250.1:p.Pro199Leu
CA361724501
NM_001375321.1:c.596C>T