Canonical Allele Identifier: PA915966904
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ser498Arg
CA3992635
NM_001079823.2:c.1494T>A
CA365607813
NM_001079823.2:c.1492A>C
CA365607818
NM_001079823.2:c.1494T>G