Canonical Allele Identifier: PA2828176296
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045744
ClinVar RCV Id: RCV002908868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Gln1041Lys
CA2094796
NM_001365521.2:c.3121C>A