Canonical Allele Identifier: PA2826176570
Gene: TMEM127 HGNC NCBI
ClinVar RCV:
RCV002628628
ClinVar Variation:
2195385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Pro233His
CA347650969
NM_001193304.3:c.698C>A