ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825361122
Gene: SCN3B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000002574
RCV000128811
RCV000171069
RCV000171567
RCV000220802
RCV000250087
ClinVar Variation:
2470
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001035241.1:p.Leu10Pro
CA163434
NM_001040151.2:c.29T>C