Canonical Allele Identifier: PA2828080960
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_001350097.1:p.Lys292Asn
CA213061
NM_001363168.1:c.876A>T
CA370405454
NM_001363168.1:c.876A>C