Canonical Allele Identifier: PA2829665733
Gene: STAMBP HGNC NCBI
ClinVar RCV:
RCV001925604
ClinVar Variation:
1412908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006454.1:p.Pro10Leu
CA1717423
NM_006463.6:c.29C>T