Canonical Allele Identifier: PA2828782681
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5926
ClinVar RCV Id: RCV000006289 RCV001851693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Gly169Arg
CA117859
NM_001378492.1:c.505G>A
CA355767178
NM_001378492.1:c.505G>C