ClinGen Allele Registry
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Canonical Allele Identifier:
PA645406817
Gene: ATP13A2
HGNC
NCBI
Linked Data
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Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_071372.1:p.Phe1051del
NM_022089.4:c.3152_3154del
NM_022089.4:c.[3152_3154del;3156T>A]
NM_022089.4:c.[3152_3154del;3156T>C]
NM_022089.4:c.[3152_3154del;3156T>G]
NM_022089.4:c.[3152_3154del;3156T=]