Canonical Allele Identifier: PA1139762013
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919539
ClinVar RCV Id: RCV001842702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1784Asp
CA352141338
NM_198056.3:c.5352G>T
CA352141339
NM_198056.3:c.5352G>C