Canonical Allele Identifier: PA265407
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67852
ClinVar RCV Id: RCV000058631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Trp1345Cys
CA017796
NM_198056.3:c.4035G>T
CA352147380
NM_198056.3:c.4035G>C