Canonical Allele Identifier: PA2828081294
Gene: VPS37A HGNC NCBI

Linked Data

ClinVar Variation Id: 522587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350101.1:p.Leu144Ile
CA4643409
NM_001363172.2:c.430C>A