Canonical Allele Identifier: PA2827050719
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13286
ClinVar RCV Id: RCV000014208 RCV000014209 RCV000256107 RCV000415503 RCV000528973 RCV003313920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ser123Cys
CA122991
NM_001320654.2:c.368C>G