Canonical Allele Identifier: PA2827609603
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 1502193
ClinVar RCV Id: RCV002020116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338361.1:p.Met121Ile
CA373835313
NM_001351432.2:c.363G>C
CA373835314
NM_001351432.2:c.363G>A
CA373835315
NM_001351432.2:c.363G>T