Canonical Allele Identifier: PA2741965548
Gene: FGF20 HGNC NCBI

Linked Data

ClinVar Variation Id: 2697660
ClinVar RCV Id: RCV003549396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062825.1:p.Ala179Ser
CA4641568
NM_019851.3:c.535G>T