Canonical Allele Identifier: PA322122
Gene: ABCB7 HGNC NCBI

Linked Data

ClinVar Variation Id: 213987
ClinVar RCV Id: RCV000197659 RCV000282088 RCV002515374 RCV003955187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004290.2:p.Trp41Arg
CA322121
NM_004299.6:c.121T>C
CA413678892
NM_004299.6:c.121T>A