Canonical Allele Identifier: PA2826712652
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1415854
ClinVar RCV Id: RCV001933289 RCV003395282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275634.1:p.Asn308Lys
CA3506989
NM_001288705.3:c.924C>G
CA361725183
NM_001288705.3:c.924C>A