ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826847579
Gene: NMNAT1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000175940
RCV001074101
RCV001256640
ClinVar Variation:
195375
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001284708.1:p.Ala13Thr
CA241796
NM_001297779.2:c.37G>A