Canonical Allele Identifier: PA159711
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 134404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000133.1:p.Phe384Leu
CA159710
NM_000142.5:c.1150T>C
CA355979069
NM_000142.5:c.1152C>A
CA355979071
NM_000142.5:c.1152C>G