Canonical Allele Identifier: PA258108
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 18079
ClinVar RCV Id: RCV000019705 RCV000335176 RCV001659725 RCV003974847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Ile70Val
CA258106
NM_001145.4:c.208A>G