Canonical Allele Identifier: PA111508
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13263
ClinVar RCV Id: RCV000014173 RCV000014174 RCV000547490 RCV000762801 RCV001730471 RCV001090933 RCV001196204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Cys342Tyr
CA280168
NM_000141.5:c.1025G>A