Canonical Allele Identifier: PA2825552987
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 406141
ClinVar RCV Id: RCV000460405 RCV000786334 RCV002356662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098679.1:p.Ala20Val
CA16611877
NM_001105209.3:c.59C>T