Canonical Allele Identifier: PA265849
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67997
ClinVar RCV Id: RCV000058791 RCV000620860 RCV003542283
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys1849Ser
CA019342
NM_000335.5:c.5546G>C
CA352140875
NM_000335.5:c.5545T>A