Canonical Allele Identifier: PA2825660375
Gene: LAMA3 HGNC NCBI
ClinVar RCV:
RCV002197374
ClinVar Variation:
1557840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121190.2:p.Gly1169Ser
CA297124538
NM_001127718.2:c.3505G>A