Canonical Allele Identifier: PA916016441
Gene: ADAMTSL2 HGNC NCBI
ClinVar RCV:
RCV000000731
ClinVar Variation:
696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055509.2:p.Gly811Arg
CA339827
NM_014694.3:c.2431G>A
CA375409420
NM_014694.3:c.2431G>C