Canonical Allele Identifier: PA2827609597
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 2444710
ClinVar RCV Id: RCV003154458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338361.1:p.Pro116Leu
CA373835342
NM_001351432.2:c.347C>T