Canonical Allele Identifier: PA2825882961
Gene: VPS37A HGNC NCBI

Linked Data

ClinVar Variation Id: 522587
ClinVar RCV Id: RCV000625725 RCV000650274 RCV001528188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138624.1:p.Leu209Ile
CA4643409
NM_001145152.2:c.625C>A