Canonical Allele Identifier: PA098979
Gene: ANG HGNC NCBI
ClinVar Allele:
33116
ClinVar RCV:
RCV000019703
ClinVar Variation:
18077
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Cys63Trp
CA258100
NM_001097577.3:c.189C>G