Canonical Allele Identifier: PA2827791130
Gene: STAMBP HGNC NCBI
ClinVar RCV:
RCV001966474
ClinVar Variation:
1467635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340897.1:p.Thr351Ser
CA1717696
NM_001353968.2:c.1052C>G
CA347293333
NM_001353968.2:c.1051A>T