Canonical Allele Identifier: PA2826302759
Gene: TMEM147 HGNC NCBI
ClinVar RCV:
RCV003681261
ClinVar Variation:
2826176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229527.1:p.His5Pro
CA405361789
NM_001242598.2:c.14A>C