Canonical Allele Identifier: PA1139672310
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 853541
ClinVar RCV Id: RCV001058369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met435Leu
CA389050909
NM_000257.4:c.1303A>T
CA389050911
NM_000257.4:c.1303A>C