Canonical Allele Identifier: PA2829346769
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002017.2:p.Tyr240Asp
CA350474250
NM_002026.4:c.718T>G