Canonical Allele Identifier: PA658662601
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 472322
ClinVar RCV Id: RCV000559654 RCV003237919 RCV003476307 RCV001011108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Ser445Leu
CA359013953
NM_004168.4:c.1334C>T