Canonical Allele Identifier: PA2828733340
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 430448
ClinVar RCV Id: RCV000494283 RCV001364718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Met358Ile
CA346501341
NM_001377959.1:c.1074G>A
CA346501342
NM_001377959.1:c.1074G>T
CA346501343
NM_001377959.1:c.1074G>C