Canonical Allele Identifier: PA916020916
Gene: PCNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161686
ClinVar RCV Id: RCV000149222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295089.1:p.Ala906Ser
CA273007
NM_001308160.2:c.2716G>T