Canonical Allele Identifier: PA112668
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 189001
ClinVar RCV Id: RCV000169383 RCV001208323 RCV001831990 RCV003468842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Arg223Trp
CA274235
NM_000478.6:c.667C>T