Canonical Allele Identifier: PA207976
Gene: ZFYVE27 HGNC NCBI

Linked Data

ClinVar Variation Id: 212641
ClinVar RCV Id: RCV000194065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002261.1:p.Thr267Met
CA207975
NM_001002261.4:c.800C>T