Canonical Allele Identifier: PA2828437080
Gene: FYN HGNC NCBI

Linked Data

ClinVar Variation Id: 98371
ClinVar RCV Id: RCV000084662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357458.1:p.Ala315Gly
CA225596
NM_001370529.1:c.944C>G