Canonical Allele Identifier: PA2829907579
Gene: TMEM242 HGNC NCBI
ClinVar RCV:
RCV004467612
ClinVar Variation:
3179258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060922.2:p.Ala6Thr
CA4068259
NM_018452.6:c.16G>A