Canonical Allele Identifier: PA2573314044
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1378047
ClinVar RCV Id: RCV003772645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1555Asp
CA352143889
NM_198056.3:c.4665G>T
CA352143890
NM_198056.3:c.4665G>C