Canonical Allele Identifier: PA2826155969
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297347
ClinVar RCV Id: RCV000361997 RCV000969136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172046.1:p.Leu13Phe
CA801486
NM_001185117.2:c.39G>T
CA339947933
NM_001185117.2:c.39G>C