Canonical Allele Identifier: PA2573100967
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1331943
ClinVar RCV Id: RCV001842173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1784Gln
CA352141351
NM_198056.3:c.5350G>C