Canonical Allele Identifier: PA891863536
Gene: EPB41L4A HGNC NCBI

Linked Data

ClinVar Variation Id: 183292
ClinVar RCV Id: RCV000162113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071423.4:p.Ser433Leu
CA186050
NM_022140.5:c.1298C>T