Canonical Allele Identifier: PA2830008581
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300
ClinVar RCV Id: RCV002513039 RCV000014227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Asp232Ala
CA280195
NM_023029.2:c.695A>C