Canonical Allele Identifier: PA2828080859
Gene: VPS37A HGNC NCBI

Linked Data

ClinVar Variation Id: 39741
ClinVar RCV Id: RCV000032956
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350096.1:p.Lys376Asn
CA213061
NM_001363167.1:c.1128A>T
CA370405454
NM_001363167.1:c.1128A>C