Canonical Allele Identifier: PA156705
Gene: AMER1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133501
ClinVar RCV Id: RCV000120005 RCV000894626 RCV000990847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689637.3:p.Ala29Thr
CA156704
NM_152424.4:c.85G>A