Canonical Allele Identifier: PA288776
Gene: COX15 HGNC NCBI

Linked Data

ClinVar Variation Id: 128836
ClinVar RCV Id: RCV000116814 RCV000259999 RCV000676871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004367.2:p.Phe374Leu
CA288774
NM_004376.7:c.1120T>C
CA378101141
NM_004376.7:c.1122T>G
CA378101142
NM_004376.7:c.1122T>A