ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825933331
Gene: SYNCRIP
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV003112544
ClinVar Variation:
2419300
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001153145.1:p.Asn145Ser
CA364905106
NM_001159673.2:c.434A>G