Canonical Allele Identifier: PA2573095397
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320736
ClinVar RCV Id: RCV001776715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Pro424Ser
CA378326972
NM_022970.3:c.1270C>T