Canonical Allele Identifier: PA1139742891
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 961207
ClinVar RCV Id: RCV001234863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met1307Ile
CA349066268
NM_001365536.1:c.3921G>T
CA349066269
NM_001365536.1:c.3921G>C
CA349066272
NM_001365536.1:c.3921G>A