Canonical Allele Identifier: PA258093
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18074
ClinVar RCV Id: RCV000019700 RCV000517735 RCV003934843 RCV001642231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Lys41Ile
CA258091
NM_001145.4:c.122A>T