Canonical Allele Identifier: PA2825480929
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 522565
ClinVar RCV Id: RCV000625710 RCV001239906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Met1323Val
CA1938645
NM_001081677.2:c.3967A>G