Canonical Allele Identifier: PA1139674616
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 976028
ClinVar RCV Id: RCV003320242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1429del
CA1139663373
NM_000257.4:c.4285_4287del