Canonical Allele Identifier: PA2828176650
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536417
ClinVar RCV Id: RCV003266301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Thr1843Ser
CA350471472
NM_001365521.2:c.5528C>G
CA350471484
NM_001365521.2:c.5527A>T