Canonical Allele Identifier: PA111879
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16349
ClinVar RCV Id: RCV000017758 RCV000623459 RCV001269614 RCV002262566 RCV002273934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000133.1:p.Asn540Ser
CA341420
NM_000142.5:c.1619A>G