Canonical Allele Identifier: PA2825933331
Gene: SYNCRIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2419300
ClinVar RCV Id: RCV003112544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153145.1:p.Asn145Ser
CA364905106
NM_001159673.2:c.434A>G