Canonical Allele Identifier: PA265873
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68001
ClinVar RCV Id: RCV000058795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Lys1872Asn
CA019389
NM_198056.3:c.5616G>C
CA352140620
NM_198056.3:c.5616G>T