Canonical Allele Identifier: PA2825944335
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2910168
ClinVar RCV Id: RCV003734579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ser941Phe
CA352140676
NM_001160161.2:c.2822C>T