Canonical Allele Identifier: PA2573213303
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 1381736
ClinVar RCV Id: RCV001922045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372203.1:p.His37Arg
CA7083140
NM_001385274.1:c.110A>G