Canonical Allele Identifier: PA2825882999
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_001138624.1:p.Lys357Asn
CA213061
NM_001145152.2:c.1071A>T
CA370405454
NM_001145152.2:c.1071A>C