Canonical Allele Identifier: PA101899
Gene: FGF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 8705
ClinVar RCV Id: RCV000009242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002001.1:p.Ser99Asn
CA119846
NM_002010.3:c.296G>A