Canonical Allele Identifier: PA2573165110
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361237
ClinVar RCV Id: RCV001907423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1103His
CA389044379
NM_000257.4:c.3309G>T
CA389044380
NM_000257.4:c.3309G>C