Canonical Allele Identifier: PA177811
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67712
ClinVar RCV Id: RCV000058479 RCV000151790 RCV000148842 RCV000157484 RCV000202895 RCV000618520 RCV000987217 RCV001149798 RCV001149799 RCV001149800 RCV001149801 RCV001149802 RCV001842310 RCV003486632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln692Lys
CA015830
NM_000335.5:c.2074C>A