Canonical Allele Identifier: PA915999513
Gene: LAMA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 713397
ClinVar RCV Id: RCV002252265 RCV004550037 RCV000885531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005550.2:p.Asp413Glu
CA8883060
NM_005559.4:c.1239C>A
CA401836189
NM_005559.4:c.1239C>G