Canonical Allele Identifier: PA2825166960
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1807348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ser541Arg
CA365608116
NM_000426.4:c.1621A>C
CA365608121
NM_000426.4:c.1623T>A
CA365608122
NM_000426.4:c.1623T>G