Canonical Allele Identifier: PA265927
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68042
ClinVar RCV Id: RCV000058845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gln270Lys
CA019808
NM_198056.3:c.808C>A