Allele Registry

Canonical Allele Identifier: PA645417201

Gene: VMA21 HGNC NCBI

ClinVar RCV:

RCV000442228

RCV000877551

RCV002525338

RCV003430988

RCV003902522

ClinVar Variation:

382097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017980.1:p.Asp5Glu	CA10540534 NM_001017980.4:c.15T>G CA415270768 NM_001017980.4:c.15T>A