Canonical Allele Identifier: PA265449
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67859
ClinVar RCV Id: RCV000058638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Lys1359Asn
CA017858
NM_198056.3:c.4077G>T
CA352147126
NM_198056.3:c.4077G>C