Canonical Allele Identifier: PA2580415955
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1910849
ClinVar RCV Id: RCV002589420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Ala43Gly
CA347656059
NM_017849.4:c.128C>G