Canonical Allele Identifier: PA2825167413
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016436
ClinVar RCV Id: RCV001315445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Phe1004Leu
CA3993128
NM_000426.4:c.3010T>C
CA365611239
NM_000426.4:c.3012C>A
CA365611240
NM_000426.4:c.3012C>G