Canonical Allele Identifier: PA2827051301
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661397
ClinVar Variation Id: 1698211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Lys657Asn
CA378314114
NM_001320658.2:c.1971G>T
CA378314117
NM_001320658.2:c.1971G>C