Canonical Allele Identifier: PA113277
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13673
ClinVar RCV Id: RCV000014664 RCV000207096 RCV000380876 RCV000724148 RCV002504786 RCV004549366
ClinVar Variation Id: 2840424
ClinVar RCV Id: RCV003716343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Phe327Leu
CA256930
NM_000478.6:c.979T>C
CA338880411
NM_000478.6:c.981C>A
CA338880412
NM_000478.6:c.981C>G