Canonical Allele Identifier: PA2828169165
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2631222
ClinVar RCV Id: RCV003404519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Asn1072Lys
CA350489080
NM_001365517.2:c.3216C>G
CA350489082
NM_001365517.2:c.3216C>A