Canonical Allele Identifier: PA2825551701
Gene: LAMA4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Ala63Glu
CA365518665
NM_001105207.3:c.188C>A