Canonical Allele Identifier: PA2830005321
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Pro263Leu
CA5720998
NM_022970.3:c.788C>T