Canonical Allele Identifier: PA658682118
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 463851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Phe173Leu
CA347652572
NM_017849.4:c.519C>G
CA347652573
NM_017849.4:c.519C>A
CA347652582
NM_017849.4:c.517T>C