Canonical Allele Identifier: PA2825924930
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695726
ClinVar RCV Id: RCV002265361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139551.1:p.Met52Ile
CA409883789
NM_001146079.2:c.156G>A
CA409883802
NM_001146079.2:c.156G>C
CA409883808
NM_001146079.2:c.156G>T