Canonical Allele Identifier: PA2825933331
Gene: SYNCRIP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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