Canonical Allele Identifier: PA1139671142
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 971190
ClinVar RCV Id: RCV001246915 RCV001788432 RCV002411908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met6Thr
CA029407
NM_000257.4:c.17T>C