Canonical Allele Identifier: PA2828179185
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444867
ClinVar RCV Id: RCV001982630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352453.1:p.Thr1840Met
CA2094033
NM_001365524.2:c.5519C>T