Canonical Allele Identifier: PA2826911862
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369933
ClinVar RCV Id: RCV001870892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Gly1037Arg
CA350489351
NM_001306130.2:c.3109G>C
CA350489352
NM_001306130.2:c.3109G>A