Canonical Allele Identifier: PA2830519875
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2322274
ClinVar RCV Id: RCV002906164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997641.2:p.Pro1076Ser
CA350489037
NM_212476.3:c.3226C>T