Canonical Allele Identifier: PA2830274330
Gene: TPCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3181495
ClinVar RCV Id: RCV004470842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620714.2:p.Asp466Asn
CA6155247
NM_139075.4:c.1396G>A