Canonical Allele Identifier: PA307363
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201469
ClinVar RCV Id: RCV000182995
ClinVar Variation Id: 1906128
ClinVar RCV Id: RCV003776596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Cys683Ser
CA015794
NM_198056.3:c.2048G>C
CA352144892
NM_198056.3:c.2047T>A