Canonical Allele Identifier: PA645397980
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 412380
ClinVar RCV Id: RCV000477192 RCV000521376 RCV001010677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.His424Gln
CA3173178
NM_004168.4:c.1272C>G
CA359013823
NM_004168.4:c.1272C>A