Canonical Allele Identifier: PA2830520887
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063372
ClinVar RCV Id: RCV001373202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997643.2:p.Lys1050Asn
CA2094790
NM_212478.3:c.3150G>C
CA350489268
NM_212478.3:c.3150G>T