Canonical Allele Identifier: PA2829722851
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695726
ClinVar RCV Id: RCV002265361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036262.1:p.Met52Ile
CA409883789
NM_012130.4:c.156G>A
CA409883802
NM_012130.4:c.156G>C
CA409883808
NM_012130.4:c.156G>T