Canonical Allele Identifier: PA225598
Gene: FYN HGNC NCBI

Linked Data

ClinVar Variation Id: 98371
ClinVar RCV Id: RCV000084662
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694592.1:p.Ala312Gly
CA225596
NM_153047.4:c.935C>G