Canonical Allele Identifier: PA111743
Gene: ELOVL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 143056
ClinVar RCV Id: RCV000132563 RCV002483274 RCV003479020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073563.1:p.Leu168Phe
CA170078
NM_022726.4:c.504G>C
CA364656512
NM_022726.4:c.504G>T