ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA302177
Gene: SCN1B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000171052
RCV002515234
ClinVar Variation:
190872
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001028.1:p.Val158Met
CA302176
NM_001037.5:c.472G>A