Canonical Allele Identifier: PA645504018
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406432
ClinVar RCV Id: RCV001841355 RCV003766543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Pro71Leu
CA16611294
NM_198056.3:c.212C>T