Canonical Allele Identifier: PA2826031042
Gene: TMEM44 HGNC NCBI

Linked Data

ClinVar Variation Id: 3179488
ClinVar RCV Id: RCV004467842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159777.1:p.Ser412Trp
CA2762538
NM_001166305.2:c.1235C>G