Canonical Allele Identifier: PA2825942529
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67977
ClinVar RCV Id: RCV000058763
ClinVar Variation Id: 446418
ClinVar RCV Id: RCV000515650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met1733Leu
CA019076
NM_001160160.2:c.5197A>C
CA352141606
NM_001160160.2:c.5197A>T