ClinGen Allele Registry
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Canonical Allele Identifier:
PA235715
Gene: SCN4B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
188498
ClinVar RCV:
RCV000171074
RCV000619132
RCV001078793
ClinVar Variation:
190891
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_777594.1:p.His65Leu
CA235713
NM_174934.4:c.194A>T