Canonical Allele Identifier: PA645485349
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 346014
ClinVar RCV Id: RCV000271632 RCV000366666 RCV001516710 RCV001753813 RCV003922518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala34Asp
CA2395047
NM_002292.4:c.101C>A