ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827609601
Gene: AUH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
976619
ClinVar RCV Id:
RCV001253975
RCV002570550
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001338361.1:p.Ala118Thr
CA5119756
NM_001351432.2:c.352G>A