Canonical Allele Identifier: PA112697
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 550442
ClinVar RCV Id: RCV001275110 RCV000665189 RCV003465439 RCV002279480 RCV000763303 RCV001050932 RCV004026080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Arg391Cys
CA666747
NM_000478.6:c.1171C>T