Canonical Allele Identifier: PA916024563
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478049
ClinVar RCV Id: RCV000534665 RCV001755916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ala86Ser
CA378328613
NM_001320654.2:c.256G>T