Canonical Allele Identifier: PA358174
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 225053
ClinVar RCV Id: RCV000210667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Pro136Ser
CA358172
NM_001145.4:c.406C>T