Canonical Allele Identifier: PA645405183
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 239116
ClinVar RCV Id: RCV000228939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Pro33Arg
CA10582439
NM_002290.4:c.98C>G