Canonical Allele Identifier: PA1139755118
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 863442
ClinVar RCV Id: RCV001070409 RCV003992439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Gln231Leu
CA405329650
NM_199037.5:c.692A>T