Canonical Allele Identifier: PA2829722873
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344633
ClinVar RCV Id: RCV001849634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036262.1:p.Ala113Pro
CA320314035
NM_012130.4:c.337G>C