Canonical Allele Identifier: PA2827651439
Gene: LINS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800392
ClinVar RCV Id: RCV002461540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339437.1:p.Lys376Asn
CA7759516
NM_001352508.2:c.1128A>C
CA393935334
NM_001352508.2:c.1128A>T