Canonical Allele Identifier: PA2825128836
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 393066
ClinVar RCV Id: RCV000441820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Trp301Cys
CA16604567
NM_000335.5:c.903G>C
CA352150377
NM_000335.5:c.903G>T