Canonical Allele Identifier: PA111890
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16344
ClinVar RCV Id: RCV000017753 RCV001549822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000133.1:p.Asn540Thr
CA341415
NM_000142.5:c.1619A>C