Canonical Allele Identifier: PA2827476754
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 2467060
ClinVar RCV Id: RCV003197005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Met1674Ile
CA2321418
NM_001349253.2:c.5022G>A
CA352161681
NM_001349253.2:c.5022G>T
CA352161685
NM_001349253.2:c.5022G>C