Canonical Allele Identifier: PA2825094939
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 876098
ClinVar RCV Id: RCV001100532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Ser512Arg
CA36756955
NM_000228.3:c.1536C>A
CA344590166
NM_000228.3:c.1536C>G
CA344590172
NM_000228.3:c.1534A>C