Canonical Allele Identifier: PA2828172916
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2491030
ClinVar RCV Id: RCV003211233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352448.1:p.Gly1071Ala
CA350489096
NM_001365519.2:c.3212G>C