Canonical Allele Identifier: PA2828177782
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352452.1:p.Cys225Trp
CA350475275
NM_001365523.2:c.675C>G