Canonical Allele Identifier: PA2580417570
Gene: PHIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1699806
ClinVar RCV Id: RCV002273663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060404.4:p.Leu155Val
CA364643371
NM_017934.7:c.463C>G