Canonical Allele Identifier: PA086936
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 222806
ClinVar RCV Id: RCV000208085 RCV002399771
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.His557Gln
CA058476
NM_198056.3:c.1671C>G
CA352146807
NM_198056.3:c.1671C>A