Canonical Allele Identifier: PA2826876237
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2126110
ClinVar RCV Id: RCV003049912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val250Leu
CA381551873
NM_001302960.2:c.748G>C
CA381551874
NM_001302960.2:c.748G>T