Canonical Allele Identifier: PA111683
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13271
ClinVar RCV Id: RCV000014190 RCV000626619 RCV000655421 RCV000726654 RCV001823713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ser347Cys
CA280173
NM_000141.5:c.1040C>G