Canonical Allele Identifier: PA2830519156
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 192244
ClinVar RCV Id: RCV000207361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997639.2:p.Trp1744Cys
CA352250
NM_212474.3:c.5232G>C
CA350471577
NM_212474.3:c.5232G>T