ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828081294
Gene: VPS37A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
522587
ClinVar RCV Id:
RCV000625725
RCV000650274
RCV001528188
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350101.1:p.Leu144Ile
CA4643409
NM_001363172.2:c.430C>A