Canonical Allele Identifier: PA2573085792
Gene: EFNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302592
ClinVar RCV Id: RCV001756266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004420.1:p.Pro34Ala
CA413437177
NM_004429.5:c.100C>G