Canonical Allele Identifier: PA2573100971
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1332221
ClinVar RCV Id: RCV001842188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Leu39Phe
CA352158790
NM_198056.3:c.117G>T
CA352158791
NM_198056.3:c.117G>C