Canonical Allele Identifier: PA2827051145
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060632
ClinVar RCV Id: RCV001370090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Asp321Val
CA378328475
NM_001320658.2:c.962A>T