Canonical Allele Identifier: PA645386487
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 279894
ClinVar RCV Id: RCV000280099 RCV000454300 RCV002251740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004773.1:p.Met1Thr