Canonical Allele Identifier: PA111349
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13269
ClinVar RCV Id: RCV000014187 RCV000014188 RCV001851846 RCV003313919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ala344Gly
CA280171
NM_000141.5:c.1031C>G