Canonical Allele Identifier: PA2828782669
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5938
ClinVar RCV Id: RCV000006301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Leu151Phe
CA355767056
NM_001378492.1:c.453G>C
CA355767057
NM_001378492.1:c.453G>T