Canonical Allele Identifier: PA645404863
Gene: NAXE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_658985.2:p.Lys245Gln
CA1162908
NM_144772.3:c.733A>C