Canonical Allele Identifier: PA2828176662
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699375
ClinVar RCV Id: RCV002273232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Leu1884Val
CA350470857
NM_001365521.2:c.5650C>G