Canonical Allele Identifier: PA2828169139
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2170043
ClinVar RCV Id: RCV003088502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Lys1050Arg
CA2094791
NM_001365517.2:c.3149A>G