Canonical Allele Identifier: PA170756
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16348
ClinVar RCV Id: RCV000017757 RCV000144153 RCV000430843 RCV000437923 RCV002228032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001156685.1:p.Lys652Gln
CA170755
NM_001163213.2:c.1954A>C