ClinGen Allele Registry
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Canonical Allele Identifier:
PA915967348
Gene: LAMA2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000520057
RCV000714624
RCV000714625
RCV001821455
ClinVar Variation:
449238
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.Asp1491Asn
CA3993565
NM_001079823.2:c.4471G>A