Canonical Allele Identifier: PA915967901
Gene: ATP2B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161476
ClinVar RCV Id: RCV000149010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001675.3:p.Asp333Glu
CA174104
NM_001684.5:c.999C>A
CA344312309
NM_001684.5:c.999C>G