Canonical Allele Identifier: PA891861029
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 570937
ClinVar RCV Id: RCV002462028 RCV001841860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp608Asn
CA058871
NM_198056.3:c.1822G>A