Canonical Allele Identifier: PA2828176352
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2961093
ClinVar RCV Id: RCV003819804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Glu1074Gly
CA350489059
NM_001365521.2:c.3221A>G