ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825168377
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000497656
RCV001361569
RCV002524079
ClinVar Variation:
432308
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000417.3:p.Leu2016Ser
CA3994082
NM_000426.4:c.6047T>C