Canonical Allele Identifier: PA2827353900
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 3178479
ClinVar RCV Id: RCV004472868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Pro312Leu
CA391203752
NM_001331238.2:c.935C>T