Canonical Allele Identifier: PA2827348551
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 2682077
ClinVar RCV Id: RCV003477369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317687.1:p.Leu499Phe
CA359014296
NM_001330758.2:c.1497G>C
CA359014297
NM_001330758.2:c.1497G>T