Canonical Allele Identifier: PA2580300144
Gene: AIP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Leu70Val
CA381547004
NM_003977.4:c.208C>G