Canonical Allele Identifier: PA2741977695
Gene: SPINT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690070
ClinVar RCV Id: RCV003486257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066925.1:p.Ser41Leu
CA9411324
NM_021102.4:c.122C>T