Canonical Allele Identifier: PA2573169359
Gene: MYL2 HGNC NCBI
ClinVar RCV:
RCV002045135
ClinVar Variation:
1502291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Asp166His
CA386696689
NM_000432.4:c.496G>C