Canonical Allele Identifier: PA645373636
Gene: EPB42 HGNC NCBI

Linked Data

ClinVar Variation Id: 255156
ClinVar RCV Id: RCV000247648 RCV000909752 RCV001116918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000110.2:p.Ser30Asn
CA7520721
NM_000119.3:c.89G>A