Canonical Allele Identifier: PA2826912955
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536417
ClinVar RCV Id: RCV003266301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Thr1752Ser
CA350471472
NM_001306131.2:c.5255C>G
CA350471484
NM_001306131.2:c.5254A>T