Canonical Allele Identifier: PA916058015
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 819022
ClinVar RCV Id: RCV001011204 RCV001058899
ClinVar Variation Id: 1405196
ClinVar RCV Id: RCV001903620 RCV002386702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Thr46Ser
CA347656042
NM_017849.4:c.137C>G
CA347656044
NM_017849.4:c.136A>T