Canonical Allele Identifier: PA2825166460
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ala5Thr
CA238603
NM_000426.4:c.13G>A