Canonical Allele Identifier: PA2828782635
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 1202637
ClinVar RCV Id: RCV001568363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Leu46Pro
CA355765476
NM_001378492.1:c.137T>C