Canonical Allele Identifier: PA2573210977
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1422507
ClinVar RCV Id: RCV001945628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met952Leu
CA349076871
NM_001365536.1:c.2854A>C
CA349076880
NM_001365536.1:c.2854A>T