Canonical Allele Identifier: PA2828172920
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719028
ClinVar RCV Id: RCV002296779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352448.1:p.Gln1073Leu
CA350489072
NM_001365519.2:c.3218A>T