Canonical Allele Identifier: PA2826517161
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1707703
ClinVar RCV Id: RCV002286682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257377.1:p.Phe579_Ter580insArgIleLeuProAlaArgAlaCysProSerTyrValProSerLeuLysProLysProLysProLeuSerLeuArgProTrpPheValProLysGlyProSerValProSerThrValProAlaLeuLysSerThrTyrCysLeuAlaAsnAsnLysAsnPhe
CA397726272
NM_001270448.2:c.1738T>C
CA397726273
NM_001270448.2:c.1738T>A