Canonical Allele Identifier: PA112652
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 521379
ClinVar RCV Id: RCV000674297 RCV000623730 RCV001046115 RCV001730702 RCV002279446 RCV003465357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Arg184Trp
CA666527
NM_000478.6:c.550C>T