Canonical Allele Identifier: PA2825381327
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 3208656
ClinVar RCV Id: RCV004502552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032728.1:p.Arg76Thr
CA2723630
NM_001037639.1:c.227G>C