Canonical Allele Identifier: PA2741893433
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2800822
ClinVar RCV Id: RCV003673741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Ala207Gly
CA345950714
NM_002381.5:c.620C>G