ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826657979
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
519022
ClinVar RCV Id:
RCV000621062
RCV001096941
RCV001096943
RCV001096942
RCV001096944
RCV001096939
RCV001096940
RCV001102354
RCV001102355
RCV000808964
RCV001190252
RCV001096945
RCV001096946
RCV001544605
RCV004002668
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269553.1:p.Val361Met
CA049885
NM_001282624.2:c.1081G>A