Canonical Allele Identifier: PA658678239
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 449199
ClinVar RCV Id: RCV000523591 RCV001841410 RCV004023536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser664Gly
CA059406
NM_198056.3:c.1990A>G