Canonical Allele Identifier: PA915965009
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193095
ClinVar RCV Id: RCV000173131 RCV000818174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ala5Thr
CA238603
NM_001079823.2:c.13G>A