Canonical Allele Identifier: PA2829373640
Gene: LAMA4 HGNC NCBI
ClinVar RCV:
RCV001967300
ClinVar Variation:
1429627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Gly1681Ser
CA3964829
NM_002290.4:c.5041G>A