Canonical Allele Identifier: PA1139762909
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 950602
ClinVar RCV Id: RCV003656586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly1863Arg
CA352140738
NM_198056.3:c.5587G>C
CA352140739
NM_198056.3:c.5587G>A