Canonical Allele Identifier: PA112786
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13679
ClinVar RCV Id: RCV000169778 RCV000710510 RCV001194283 RCV001253058 RCV000014672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Asn417Ser
CA199266
NM_000478.6:c.1250A>G