Canonical Allele Identifier: PA2826911288
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Ile1921Phe
CA2094035
NM_001306129.2:c.5761A>T