Canonical Allele Identifier: PA645414866
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235025
ClinVar RCV Id: RCV000223772 RCV003586169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro402Ser
CA10581178
NM_000257.4:c.1204C>T