Canonical Allele Identifier: PA1139722474
Gene: NSUN2 HGNC NCBI
ClinVar RCV:
RCV001249286
ClinVar Variation:
972974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060225.4:p.Val676Ile
CA3192204
NM_017755.6:c.2026G>A