Canonical Allele Identifier: PA1139729381
Gene: PRKN HGNC NCBI

Linked Data

ClinVar Variation Id: 854929
ClinVar RCV Id: RCV001060078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054643.2:p.Glu49Asp
CA366477221
NM_013988.3:c.147G>T
CA366477222
NM_013988.3:c.147G>C