Canonical Allele Identifier: PA2573293056
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390835
ClinVar RCV Id: RCV001891203
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Val66Ala
CA380970188
NM_032667.6:c.197T>C