Canonical Allele Identifier: PA2827609595
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 1905499
ClinVar RCV Id: RCV002588801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338361.1:p.Gly111Arg
CA373835376
NM_001351432.2:c.331G>C
CA373835377
NM_001351432.2:c.331G>A