ClinGen Allele Registry
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Canonical Allele Identifier:
PA915967470
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
98876
ClinVar RCV:
RCV000078780
RCV000872576
RCV001152796
RCV001719818
ClinVar Variation:
92969
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.Ser1878Phe
CA146142
NM_001079823.2:c.5633C>T