Canonical Allele Identifier: PA2580140172
Gene: LINS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800392
ClinVar RCV Id: RCV002461540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035706.2:p.Lys391Asn
CA7759516
NM_001040616.3:c.1173A>C
CA393935334
NM_001040616.3:c.1173A>T