Canonical Allele Identifier: PA2573168274
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1359321
ClinVar RCV Id: RCV001872224
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1566Ser
CA400615385
NM_000334.4:c.4696G>A