Canonical Allele Identifier: PA2580154198
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_001159778.1:p.Met356Ile
CA2762546
NM_001166306.2:c.1068G>C
CA355824972
NM_001166306.2:c.1068G>T
CA355824973
NM_001166306.2:c.1068G>A