Canonical Allele Identifier: PA645405768
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 406146
ClinVar RCV Id: RCV000475717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Asp1739Gly
CA16612096
NM_002290.4:c.5216A>G