Canonical Allele Identifier: PA2741891819
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2750007
ClinVar RCV Id: RCV003582826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Leu15Phe
CA365518961
NM_002290.4:c.43C>T