Canonical Allele Identifier: PA2580179880
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_001240700.1:p.Asn91Ser
CA364905106
NM_001253771.2:c.272A>G