Canonical Allele Identifier: PA2828175282
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699375
ClinVar RCV Id: RCV002273232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352449.1:p.Leu1883Val
CA350470857
NM_001365520.2:c.5647C>G