Canonical Allele Identifier: PA645404894
Gene: NAXE HGNC NCBI

Linked Data

ClinVar Variation Id: 268119
ClinVar RCV Id: RCV000258817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_658985.2:p.Lys270del
CA10602659
NM_144772.3:c.804_807delinsA
CA31066323
NM_144772.3:c.808_810del