Canonical Allele Identifier: PA658670871
Gene: HAX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476636
ClinVar RCV Id: RCV000556301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006109.2:p.Asp5Ala
CA1127208
NM_006118.4:c.14A>C