Canonical Allele Identifier: PA658814553
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 541218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Leu1517Phe
CA3964958
NM_002290.4:c.4551G>C
CA365369588
NM_002290.4:c.4551G>T