Allele Registry

Canonical Allele Identifier: PA645386507

Gene: SNAP29 HGNC NCBI

ClinVar RCV:

RCV000367997

RCV003243096

ClinVar Variation:

340835

HGVS (amino-acid)	Matching Registered Transcripts
NP_004773.1:p.Met184Val	CA10117180 NM_004782.4:c.550A>G