Canonical Allele Identifier: PA645438675
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 307213
ClinVar RCV Id: RCV000278835 RCV001181051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Asn101Ser
CA10640938
NM_000432.4:c.302A>G