Canonical Allele Identifier: PA916024569
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374815
ClinVar RCV Id: RCV000415483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Asp336Gly
CA16043913
NM_001320658.2:c.1007A>G