Canonical Allele Identifier: PA2825306787
Gene: TMEM44 HGNC NCBI

Linked Data

ClinVar Variation Id: 2543855
ClinVar RCV Id: RCV004314566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011655.1:p.Val369Ile
CA2762535
NM_001011655.2:c.1105G>A