Canonical Allele Identifier: PA112635
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13675
ClinVar RCV Id: RCV000014666 RCV000169168 RCV000364426 RCV000767525 RCV000770988 RCV002276548 RCV002490366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Arg136His
CA256932
NM_000478.6:c.407G>A