Canonical Allele Identifier: PA2828807162
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1948344
ClinVar RCV Id: RCV002667664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.His1469Tyr
CA372965987
NM_001379081.2:c.4405C>T