Canonical Allele Identifier: PA2825315565
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1199377
ClinVar RCV Id: RCV001563997 RCV001563998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Pro576Leu
CA1375480
NM_001017402.2:c.1727C>T