ClinGen Allele Registry
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Canonical Allele Identifier:
PA214231
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000030432
RCV000079572
RCV000338109
RCV000401331
RCV000860058
RCV001132319
RCV002311528
ClinVar Variation:
36753
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001159435.1:p.Ala1067Thr
CA214227
NM_001165963.4:c.3199G>A