Canonical Allele Identifier: PA1139690173
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 988310
ClinVar RCV Id: RCV001269575
ClinVar Variation Id: 1684537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001156685.1:p.Val557Leu
CA355981675
NM_001163213.2:c.1669G>C
CA355981676
NM_001163213.2:c.1669G>T