Canonical Allele Identifier: PA2826184577
Gene: NSUN2 HGNC NCBI
ClinVar RCV:
RCV001249286
ClinVar Variation:
972974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180384.1:p.Val641Ile
CA3192204
NM_001193455.2:c.1921G>A