Canonical Allele Identifier: PA2830099231
Gene: ABCC11 HGNC NCBI

Linked Data

ClinVar Variation Id: 779015
ClinVar RCV Id: RCV000959760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149163.2:p.Val491Ile
CA8043868
NM_033151.4:c.1471G>A