Canonical Allele Identifier: PA891851557
Gene: LAMA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 587464
ClinVar RCV Id: RCV000714632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005550.2:p.Pro1018Ala
CA8882415
NM_005559.4:c.3052C>G