Canonical Allele Identifier: PA107991
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67698
ClinVar RCV Id: RCV000058462 RCV000171572 RCV001842303 RCV003764734 RCV003298119 RCV004528264
ClinVar Variation Id: 67699
ClinVar RCV Id: RCV000058463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly639Arg
CA015554
NM_198056.3:c.1915G>A
CA015563
NM_198056.3:c.1915G>C