Canonical Allele Identifier: PA916076081
Gene: ABCC11 HGNC NCBI
ClinVar RCV:
RCV000959760
ClinVar Variation:
779015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660187.1:p.Val491Ile
CA8043868
NM_145186.3:c.1471G>A