Canonical Allele Identifier: PA126934
Gene: ALAD HGNC NCBI

Linked Data

ClinVar Variation Id: 16864
ClinVar RCV Id: RCV000018360 RCV000371179 RCV001509916 RCV002247353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000022.3:p.Lys59Asn
CA126933
NM_000031.6:c.177G>C
CA374565189
NM_000031.6:c.177G>T