ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139689420
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000591454
RCV001081139
RCV001154299
RCV004541463
ClinVar Variation:
242607
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000417.3:p.Ile2761Thr
CA051962
NM_000426.4:c.8282T>C