Canonical Allele Identifier: PA2827568478
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 375370
ClinVar RCV Id: RCV000416463 RCV001092912 RCV002521493
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337677.1:p.Ile322Thr
CA16044232
NM_001350748.2:c.965T>C