Canonical Allele Identifier: PA916024557
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374812
ClinVar RCV Id: RCV000415506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Trp62Ser
CA16043916
NM_001320654.2:c.185G>C