Canonical Allele Identifier: PA916024543
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13285
ClinVar RCV Id: RCV000014207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Val41_Val42del
CA10575516
NM_001320654.2:c.120_125del