Canonical Allele Identifier: PA2499237264
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016436
ClinVar RCV Id: RCV001315445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Phe1004Leu
CA3993128
NM_001079823.2:c.3010T>C
CA365611239
NM_001079823.2:c.3012C>A
CA365611240
NM_001079823.2:c.3012C>G