Canonical Allele Identifier: PA913201044
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191678
ClinVar RCV Id: RCV000171966 RCV000692677 RCV000769186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098676.2:p.Gly1813Ser
CA237245
NM_001105206.3:c.5437G>A