Canonical Allele Identifier: PA2829368012
Gene: JUP HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Gln17Lys
CA399507207
NM_002230.4:c.49C>A