Canonical Allele Identifier: PA2580195437
Gene: FARP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2488030
ClinVar RCV Id: RCV004275629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273768.1:p.Ser1061Phe
CA388592695
NM_001286839.2:c.3182C>T