Canonical Allele Identifier: PA156701
Gene: AMER1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689637.3:p.Ala264Thr
CA156700
NM_152424.4:c.790G>A