Canonical Allele Identifier: PA2825352578
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 651308
ClinVar RCV Id: RCV000806634 RCV003238818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Phe86Leu
CA405328631
NM_001037.5:c.256T>C
CA405328640
NM_001037.5:c.258C>A
CA405328642
NM_001037.5:c.258C>G