Canonical Allele Identifier: PA2825132329
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519384
ClinVar RCV Id: RCV000620538 RCV003656130
ClinVar Variation Id: 2027600
ClinVar RCV Id: RCV003658312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1765Ile
CA352141596
NM_000335.5:c.5295G>A
CA352141598
NM_000335.5:c.5295G>T
CA352141600
NM_000335.5:c.5295G>C