Canonical Allele Identifier: PA129947
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16359
ClinVar RCV Id: RCV000017770 RCV000029208 RCV000413645 RCV000443051 RCV003493410 RCV003989295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001156685.1:p.Gly372Cys
CA129946
NM_001163213.2:c.1114G>T