Canonical Allele Identifier: PA2825109897
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072367
ClinVar RCV Id: RCV004012397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe456Ser
CA389050774
NM_000257.4:c.1367T>C