Canonical Allele Identifier: PA2827353897
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2281864
ClinVar RCV Id: RCV004137952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Met309Ile
CA391203709
NM_001331238.2:c.927G>A
CA391203711
NM_001331238.2:c.927G>C
CA391203714
NM_001331238.2:c.927G>T