Canonical Allele Identifier: PA111911
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000133.1:p.Gly370Cys
CA129946
NM_000142.5:c.1108G>T