Canonical Allele Identifier: PA2827299640
Gene: GLDN HGNC NCBI

Linked Data

ClinVar Variation Id: 452116
ClinVar RCV Id: RCV000524042 RCV000855464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317226.1:p.Phe352Leu
CA7560758
NM_001330297.2:c.1056C>A
CA392435275
NM_001330297.2:c.1054T>C
CA392435286
NM_001330297.2:c.1056C>G