Canonical Allele Identifier: PA2825219875
Gene: FOLR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2599845
ClinVar RCV Id: RCV004343328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000794.3:p.Leu28Phe
CA6169317
NM_000803.5:c.82C>T