Canonical Allele Identifier: PA2573314588
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1475237
ClinVar RCV Id: RCV001976089
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Asp175Glu
CA405329235
NM_199037.5:c.525C>A
CA405329236
NM_199037.5:c.525C>G