Canonical Allele Identifier: PA2825494662
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1176454
ClinVar RCV Id: RCV001531992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Phe934Leu
CA352140760
NM_001099405.2:c.2802C>G
CA352140761
NM_001099405.2:c.2802C>A
CA352140771
NM_001099405.2:c.2800T>C