Canonical Allele Identifier: PA073412
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 222803
ClinVar RCV Id: RCV000208042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser262Arg
CA073231
NM_198056.3:c.784A>C
CA352150763
NM_198056.3:c.786C>A
CA352150766
NM_198056.3:c.786C>G