Canonical Allele Identifier: PA2741904376
Gene: CILP HGNC NCBI
ClinVar RCV:
RCV004325320
ClinVar Variation:
2557522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003604.4:p.Val135Leu
CA271514188
NM_003613.4:c.403G>T
CA392874010
NM_003613.4:c.403G>C