Canonical Allele Identifier: PA184602
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67802
ClinVar RCV Id: RCV000058576 RCV000156315 RCV001150963 RCV000765735 RCV001150965 RCV001150967 RCV001150964 RCV001150966 RCV001150968 RCV001842338 RCV003654192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala1186Thr
CA017261
NM_198056.3:c.3556G>A