Canonical Allele Identifier: PA296974
Gene: MYL2 HGNC NCBI
ClinVar RCV:
RCV000158935
ClinVar Variation:
181436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Asp166Tyr
CA010463
NM_000432.4:c.496G>T