Canonical Allele Identifier: PA2827255496
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 218097
ClinVar RCV Id: RCV000202343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311367.1:p.Ser77Asn
CA248581
NM_001324438.2:c.230G>A