ClinGen Allele Registry
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Canonical Allele Identifier:
PA915965084
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000518765
RCV000654769
RCV001154065
RCV001508564
ClinVar Variation:
447689
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.Ala1897Thr
CA3993954
NM_001079823.2:c.5689G>A