Canonical Allele Identifier: PA2828176661
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2238487
ClinVar RCV Id: RCV002729256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Ile1882Phe
CA350470888
NM_001365521.2:c.5644A>T