Canonical Allele Identifier: PA151158
Gene: BCS1L HGNC NCBI
ClinVar RCV:
RCV000114392
ClinVar Variation:
126497
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004319.1:p.Tyr301Asn
CA151154
NM_004328.5:c.901T>A