Canonical Allele Identifier: PA341254
Gene: EPB42 HGNC NCBI

Linked Data

ClinVar Variation Id: 13233
ClinVar RCV Id: RCV000014138 RCV003415697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000110.2:p.Ala142Thr
CA341253
NM_000119.3:c.424G>A