Canonical Allele Identifier: PA2830008711
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374818
ClinVar RCV Id: RCV000415501 RCV001270790 RCV001591054 RCV001861462
ClinVar Variation Id: 2131381
ClinVar RCV Id: RCV003048177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Cys253Gly
CA16043910
NM_023029.2:c.757T>G
CA2580082429
NM_023029.2:c.756_757delinsAG