Canonical Allele Identifier: PA2828782622
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 344447
ClinVar RCV Id: RCV000346413 RCV000974602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Phe15Leu
CA2753733
NM_001378492.1:c.45C>G
CA355762628
NM_001378492.1:c.43T>C
CA355762632
NM_001378492.1:c.45C>A