Canonical Allele Identifier: PA2828679377
Gene: SNAP91 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363640.1:p.Pro675Ser
CA3908187
NM_001376711.1:c.2023C>T