Canonical Allele Identifier: PA263492
Gene: PPT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56187
ClinVar RCV Id: RCV000049598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000301.1:p.Gln91Pro
CA263490
NM_000310.4:c.272A>C