Canonical Allele Identifier: PA2580572217
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2322274
ClinVar RCV Id: RCV002906164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997647.2:p.Pro1076Ser
CA350489037
NM_212482.4:c.3226C>T