Canonical Allele Identifier: PA2826540655
Gene: TAMALIN HGNC NCBI

Linked Data

ClinVar Variation Id: 221938
ClinVar RCV Id: RCV000207395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258785.1:p.Gly219Ser
CA072379
NM_001271856.2:c.655G>A