Canonical Allele Identifier: PA2825094981
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 723816
ClinVar RCV Id: RCV000897632 RCV002539458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Leu559Phe
CA1375496
NM_000228.3:c.1677G>T
CA344589849
NM_000228.3:c.1677G>C