Canonical Allele Identifier: PA2830274331
Gene: TPCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3181496
ClinVar RCV Id: RCV004470843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620714.2:p.Val503Met
CA6155288
NM_139075.4:c.1507G>A