Canonical Allele Identifier: PA301921
Gene: CASQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 190750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001223.2:p.Tyr12Asn
CA301919
NM_001232.4:c.34T>A