Canonical Allele Identifier: PA2825942645
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 392829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asn1804Lys
CA16604559
NM_001160160.2:c.5412C>A
CA352140956
NM_001160160.2:c.5412C>G