Canonical Allele Identifier: PA2825660085
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2084620
ClinVar RCV Id: RCV003011231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121190.2:p.Lys566Asn
CA8916456
NM_001127718.2:c.1698G>T
CA402051442
NM_001127718.2:c.1698G>C