Canonical Allele Identifier: PA2580300196
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2126110
ClinVar RCV Id: RCV003049912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Val250Leu
CA381551873
NM_003977.4:c.748G>C
CA381551874
NM_003977.4:c.748G>T