Canonical Allele Identifier: PA658804527
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518774
ClinVar RCV Id: RCV000618173 RCV001868100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1583Leu
CA389037719
NM_000257.4:c.4747A>T
CA389037721
NM_000257.4:c.4747A>C