Canonical Allele Identifier: PA2828170961
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2844199
ClinVar RCV Id: RCV003716725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352447.1:p.Ala1059Val
CA350489215
NM_001365518.2:c.3176C>T