Canonical Allele Identifier: PA107646
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9385
ClinVar RCV Id: RCV000009983 RCV000058705 RCV000183084 RCV001329632 RCV004528098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp1595Asn
CA018551
NM_198056.3:c.4783G>A