Canonical Allele Identifier: PA2828782670
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 974421
ClinVar RCV Id: RCV001281173 RCV001879805 RCV002570440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Asn153Ser
CA2753877
NM_001378492.1:c.458A>G