Canonical Allele Identifier: PA2830521230
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699375
ClinVar RCV Id: RCV002273232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997643.2:p.Leu1883Val
CA350470857
NM_212478.3:c.5647C>G