Canonical Allele Identifier: PA2829658389
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_006363.4:p.Asn243Ser
CA364905106
NM_006372.5:c.728A>G