Canonical Allele Identifier: PA916024569
Gene: FGFR2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Asp336Gly
CA16043913
NM_001320658.2:c.1007A>G