Canonical Allele Identifier: PA2828178087
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063372
ClinVar RCV Id: RCV001373202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352452.1:p.Lys1050Asn
CA2094790
NM_001365523.2:c.3150G>C
CA350489268
NM_001365523.2:c.3150G>T