Canonical Allele Identifier: PA916047615
Gene: CPS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 544153
ClinVar RCV Id: RCV000655213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356185.1:p.Met803Ile
CA350439808
NM_001369256.1:c.2409G>A
CA350439809
NM_001369256.1:c.2409G>C
CA350439810
NM_001369256.1:c.2409G>T