Canonical Allele Identifier: PA114687
Gene: ARMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 979
ClinVar RCV Id: RCV000001030 RCV000190307 RCV003982819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093137.1:p.Ala69Ser
CA114686
NM_001099667.3:c.205G>T