Canonical Allele Identifier: PA658800376
Gene: SH3PXD2B HGNC NCBI

Linked Data

ClinVar Variation Id: 501675
ClinVar RCV Id: RCV000591785 RCV000764589 RCV004024825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017995.1:p.Pro730Leu
CA3561020
NM_001017995.3:c.2189C>T