Canonical Allele Identifier: PA2573300635
Gene: NAXE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_658985.2:p.Met104Leu
CA31065604
NM_144772.3:c.310A>C
CA342872762
NM_144772.3:c.310A>T