Canonical Allele Identifier: PA346508
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 180433
ClinVar RCV Id: RCV000157352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr265Ser
CA016835
NM_000257.4:c.793A>T
CA389052039
NM_000257.4:c.794C>G