Canonical Allele Identifier: PA2828081449
Gene: VPS37A HGNC NCBI
ClinVar RCV:
RCV000032956
ClinVar Variation:
39741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350102.1:p.Lys382Asn
CA213061
NM_001363173.2:c.1146A>T
CA370405454
NM_001363173.2:c.1146A>C