Canonical Allele Identifier: PA2825306780
Gene: TMEM44 HGNC NCBI

Linked Data

ClinVar Variation Id: 2343392
ClinVar RCV Id: RCV004181538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011655.1:p.Ala358Pro
CA2762546
NM_001011655.2:c.1072G>C