Canonical Allele Identifier: PA2830432406
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072997
ClinVar RCV Id: RCV004015011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Phe1617Leu
CA352143086
NM_198056.3:c.4851C>G
CA352143087
NM_198056.3:c.4851C>A
CA352143093
NM_198056.3:c.4849T>C