Canonical Allele Identifier: PA2827073646
Gene: EXOC6B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308658.1:p.Ile448Val
CA347429679
NM_001321729.2:c.1342A>G