Canonical Allele Identifier: PA2829373410
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 488160
ClinVar RCV Id: RCV000578048 RCV000578098 RCV000578116 RCV000577985 RCV000578042 RCV000951026 RCV003159972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Ile1241Val
CA3965136
NM_002290.4:c.3721A>G