Canonical Allele Identifier: PA307297
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2089206
ClinVar RCV Id: RCV003658492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser528Arg
CA015016
NM_198056.3:c.1584C>A
CA352147346
NM_198056.3:c.1584C>G
CA352147368
NM_198056.3:c.1582A>C