Canonical Allele Identifier: PA1139763111
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 978333
ClinVar RCV Id: RCV001256854 RCV002486000 RCV004004926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1938Asp
CA352139848
NM_198056.3:c.5814A>T
CA352139850
NM_198056.3:c.5814A>C