Canonical Allele Identifier: PA108155
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67816
ClinVar RCV Id: RCV000058591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Lys1236Asn
CA017441
NM_198056.3:c.3708G>T
CA352149346
NM_198056.3:c.3708G>C