Canonical Allele Identifier: PA2828172890
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352448.1:p.Lys1050Thr
CA2094792
NM_001365519.2:c.3149A>C