Canonical Allele Identifier: PA645424896
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_683763.2:p.Leu13Phe
CA801486
NM_148960.3:c.39G>T
CA339947933
NM_148960.3:c.39G>C