Allele Registry

Canonical Allele Identifier: PA121639

Gene: EFNB1 HGNC NCBI

ClinVar RCV:

RCV000012479

ClinVar Variation:

11713

HGVS (amino-acid)	Matching Registered Transcripts
NP_004420.1:p.Trp37Gly	CA121638 NM_004429.5:c.109T>G