Canonical Allele Identifier: PA2830087575
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 305179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Ala185Ser
CA10638912
NM_032667.6:c.553G>T