Canonical Allele Identifier: PA2830374276
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 2447643
ClinVar RCV Id: RCV003176551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Val152Ala
CA6300213
NM_174934.4:c.455T>C