Canonical Allele Identifier: PA174785
Gene: DGCR6L HGNC NCBI

Linked Data

ClinVar Variation Id: 161788
ClinVar RCV Id: RCV000149324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_150282.2:p.Pro203Leu
CA174784
NM_033257.4:c.608C>T