Allele Registry

Canonical Allele Identifier: PA111868

Gene: FGFR3 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000017740

RCV000017741

RCV000255372

RCV000255928

RCV000353403

RCV000415460

RCV000622950

RCV000763122

RCV001332222

RCV001804740

RCV002273932

RCV002276553

RCV004541008

ClinVar Variation:

16337

16338

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000133.1:p.Asn540Lys	CA341410 NM_000142.5:c.1620C>A CA341412 NM_000142.5:c.1620C>G