Canonical Allele Identifier: PA2826536878
Gene: ABCB7 HGNC NCBI

Linked Data

ClinVar Variation Id: 213987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258626.1:p.Trp41Arg
CA322121
NM_001271697.2:c.121T>C
CA413678892
NM_001271697.2:c.121T>A