Canonical Allele Identifier: PA113397
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13668
ClinVar RCV Id: RCV000014656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Tyr436His
CA256925
NM_000478.6:c.1306T>C