Canonical Allele Identifier: PA098988
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18073
ClinVar RCV Id: RCV000019699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Gln36Leu
CA258088
NM_001097577.3:c.107A>T