Canonical Allele Identifier: PA2580168165
Gene: SH3D21 HGNC NCBI

Linked Data

ClinVar Variation Id: 2476396
ClinVar RCV Id: RCV004271122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001156002.1:p.Val53Met
CA339405006
NM_001162530.1:c.157G>A