Canonical Allele Identifier: PA2829405504
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_002492.2:p.Met48Lys
CA404313335
NM_002501.4:c.143T>A