Canonical Allele Identifier: PA2826361109
Gene: ERBIN HGNC NCBI

Linked Data

ClinVar Variation Id: 161721
ClinVar RCV Id: RCV000149257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240630.1:p.Tyr1248Phe
CA174662
NM_001253701.2:c.3743A>T