Canonical Allele Identifier: PA2825793761
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 2862356
ClinVar RCV Id: RCV003699809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136.1:p.Phe124Ile
CA7083186
NM_001145.4:c.370T>A