Canonical Allele Identifier: PA2828806905
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2547239
ClinVar RCV Id: RCV003273020
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Asp554Val
CA372960148
NM_001379081.2:c.1661A>T