Canonical Allele Identifier: PA2825793719
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2212376
ClinVar RCV Id: RCV002677396 RCV003574981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Gln43His
CA7083141
NM_001145.4:c.129G>C
CA389114220
NM_001145.4:c.129G>T