Canonical Allele Identifier: PA2828782653
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5934
ClinVar RCV Id: RCV000006297 RCV001093267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Leu81Phe
CA117867
NM_001378492.1:c.243G>T
CA355766002
NM_001378492.1:c.243G>C