Canonical Allele Identifier: PA174663
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_061165.1:p.Tyr1252Phe
CA174662
NM_018695.4:c.3755A>T