Canonical Allele Identifier: PA2825166914
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642364
ClinVar RCV Id: RCV000795818 RCV003133609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ser498Arg
CA3992635
NM_000426.4:c.1494T>A
CA365607813
NM_000426.4:c.1492A>C
CA365607818
NM_000426.4:c.1494T>G