Canonical Allele Identifier: PA2829061773
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 199176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Pro367Leu
CA248240
NM_001386028.1:c.1100C>T