Canonical Allele Identifier: PA114460
Gene: TPCN2 HGNC NCBI
ClinVar RCV:
RCV000000764
ClinVar Variation:
728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620714.2:p.Gly734Glu
CA114459
NM_139075.4:c.2201G>A