Canonical Allele Identifier: PA2826912709
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063372
ClinVar RCV Id: RCV001373202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Lys1050Asn
CA2094790
NM_001306131.2:c.3150G>C
CA350489268
NM_001306131.2:c.3150G>T