Canonical Allele Identifier: PA111551
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374817
ClinVar RCV Id: RCV000415513 RCV000762802 RCV001377881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Gly338Glu
CA16043911
NM_000141.5:c.1013G>A