ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645441190
Gene: SDHD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
412513
ClinVar RCV Id:
RCV001022846
RCV003103788
RCV004002010
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002993.1:p.Met155Lys
CA16613468
NM_003002.4:c.464T>A