ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827051190
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1373931
ClinVar RCV Id:
RCV001877561
RCV002482591
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001307587.1:p.Pro413Leu
CA5720813
NM_001320658.2:c.1238C>T