Canonical Allele Identifier: PA1139760135
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 920152
ClinVar RCV Id: RCV001842745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asn958Ser
CA352140425
NM_198056.3:c.2873A>G