Canonical Allele Identifier: PA915979811
Gene: PPT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56207
ClinVar RCV Id: RCV000049618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136076.1:p.Pro86Arg
CA263534
NM_001142604.2:c.257C>G