Canonical Allele Identifier: PA2830087150
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3234754
ClinVar RCV Id: RCV004547102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Met1Ile
CA380970837
NM_032667.6:c.3G>T
CA380970838
NM_032667.6:c.3G>C
CA380970839
NM_032667.6:c.3G>A