Canonical Allele Identifier: PA173824
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 160230
ClinVar RCV Id: RCV000147894 RCV000731958 RCV004532662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995584.1:p.Val143Leu
CA173822
NM_205862.3:c.427G>T
CA351074993
NM_205862.3:c.427G>C