Allele Registry

Canonical Allele Identifier: PA645453299

Gene: SCN4A HGNC NCBI

Linked Data

ClinVar RCV:

RCV000252827

RCV000282590

RCV000297937

RCV000394071

RCV000398536

RCV000513070

RCV001083859

RCV004529423

ClinVar Variation:

255852

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Met135Leu	CA8710164 NM_000334.4:c.403A>C CA400639743 NM_000334.4:c.403A>T