Canonical Allele Identifier: PA2830034179
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 3178479
ClinVar RCV Id: RCV004472868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079544.1:p.Pro312Leu
CA391203752
NM_025268.4:c.935C>T