Canonical Allele Identifier: PA2825871980
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093701
ClinVar RCV Id: RCV002996861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Cys253del
CA378327957
NM_001144915.2:c.759C>A
CA2580082428
NM_001144915.2:c.758_760del