Canonical Allele Identifier: PA1139752979
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 994398
ClinVar RCV Id: RCV001287748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_652763.1:p.Val144Met
CA10019258
NM_144492.3:c.430G>A