Canonical Allele Identifier: PA2830008483
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316322
ClinVar RCV Id: RCV001766228 RCV002488617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Gly172Arg
CA378331011
NM_023029.2:c.514G>C
CA378331012
NM_023029.2:c.514G>A