Canonical Allele Identifier: PA2826875508
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2126110
ClinVar RCV Id: RCV003049912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Val191Leu
CA381551873
NM_001302959.2:c.571G>C
CA381551874
NM_001302959.2:c.571G>T