Canonical Allele Identifier: PA2825166521
Gene: LAMA2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Met65Lys
CA365828558
NM_000426.4:c.194T>A