Canonical Allele Identifier: PA2825475001
Gene: CPSF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2491272
ClinVar RCV Id: RCV004280266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075028.1:p.Val153Ala
CA368346909
NM_001081559.3:c.458T>C