Canonical Allele Identifier: PA2827051300
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376153
ClinVar RCV Id: RCV000417597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Lys657Glu
CA16602610
NM_001320658.2:c.1969A>G