Canonical Allele Identifier: PA159712
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 134404
ClinVar RCV Id: RCV000121079 RCV000442867 RCV000987395 RCV002277184 RCV002483215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001156685.1:p.Phe386Leu
CA159710
NM_001163213.2:c.1156T>C
CA355979069
NM_001163213.2:c.1158C>A
CA355979071
NM_001163213.2:c.1158C>G