Canonical Allele Identifier: PA2828074745
Gene: PHF20L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2318021
ClinVar RCV Id: RCV004163729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349900.1:p.Ile15Phe
CA372222291
NM_001362971.2:c.43A>T