Canonical Allele Identifier: PA2741875522
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2641895
ClinVar RCV Id: RCV003395882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Ala35Ser
CA380971110
NM_001386028.1:c.103G>T