Canonical Allele Identifier: PA2830520166
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_997641.2:p.Leu1793Val
CA350470857
NM_212476.3:c.5377C>G