Canonical Allele Identifier: PA115647
Gene: NPC1L1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037521.2:p.Val55Leu
CA115646
NM_013389.3:c.163G>T
CA4242524
NM_013389.3:c.163G>C