Canonical Allele Identifier: PA2828782778
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5933
ClinVar RCV Id: RCV000006296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365422.1:p.Ser165Phe
CA117866
NM_001378493.1:c.494C>T