Canonical Allele Identifier: PA658675282
Gene: NFIX HGNC NCBI

Linked Data

ClinVar Variation Id: 452926
ClinVar RCV Id: RCV000519161 RCV001263215 RCV003766975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257972.1:p.Met56Lys
CA404313335
NM_001271043.2:c.167T>A