Canonical Allele Identifier: PA916058027
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 819465
ClinVar RCV Id: RCV001012029 RCV001216559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Pro51Leu
CA347656013
NM_017849.4:c.152C>T