Canonical Allele Identifier: PA645386529
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 436825
ClinVar RCV Id: RCV000500650 RCV001507497 RCV003960183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004773.1:p.Ser210Phe
CA10117218
NM_004782.4:c.629C>T