Canonical Allele Identifier: PA2827353898
Gene: TMEM121 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606763
ClinVar RCV Id: RCV004349032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001318167.1:p.Ser310Phe
CA266602569
NM_001331238.2:c.929C>T