Canonical Allele Identifier: PA101098
Gene: VPS37A HGNC NCBI

Linked Data

ClinVar Variation Id: 39741
ClinVar RCV Id: RCV000032956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689628.2:p.Lys382Asn
CA213061
NM_152415.3:c.1146A>T
CA370405454
NM_152415.3:c.1146A>C