Canonical Allele Identifier: PA2828171663
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 192245
ClinVar RCV Id: RCV000207403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352447.1:p.Leu1883Pro
CA352252
NM_001365518.2:c.5648T>C