Canonical Allele Identifier: PA2825494689
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ser941Asn
CA016545
NM_001099405.2:c.2821_2822delinsAA