Canonical Allele Identifier: PA2826912164
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444867
ClinVar RCV Id: RCV001982630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Thr1841Met
CA2094033
NM_001306130.2:c.5522C>T