Canonical Allele Identifier: PA2828487794
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1369594
ClinVar RCV Id: RCV001894932 RCV002490047
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358372.1:p.Gln195His
CA2109699
NM_001371443.1:c.585G>C
CA350627434
NM_001371443.1:c.585G>T