Canonical Allele Identifier: PA2825945716
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1978233
ClinVar RCV Id: RCV003658132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly1812Arg
CA352140702
NM_001160161.2:c.5434G>C
CA352140703
NM_001160161.2:c.5434G>A